CDRHNew - News and Updates
A comprehensive list of the latest CDRH updates.
This Week in CDRH
February 23, 2023
- Revised Emergency Use Authorizations
- Consumer Information on: Guardant360 CDx - P200010/S010
February 22, 2023
- New Emergency Use Authorization
- At-Home OTC COVID-19 Diagnostic Tests (Updated)
- Evaluation of Automatic Class III Designation (De Novo) Summaries (DEN210022 added)
- CDRH Learn (Updated)
- Presentation, Transcript, and Printable Slides: Virtual Town Hall Series - Test Development and Validation During Public Health Emergencies Monkeypox (mpox) and COVID-19 - February 15, 2023
- ASCA-Accredited Testing Laboratories (Updated)
February 21, 2023
- New Emergency Use Authorization
- Revised Emergency Use Authorization
- Reissued Emergency Use Authorizations
- Terminated Emergency Use Authorization
- Appendix A: Authorized Molecular-Based Laboratory Developed Tests for Detection of Nucleic Acid from SARS-CoV-2 (Updated)
- Laser Products - Conformance with IEC 60825-1 Ed. 3 and IEC 60601-2-22 Ed. 3.1 (Laser Notice No. 56) - Guidance for Industry and Food and Drug Administration Staff
- Medical X-Ray Imaging Devices Conformance with IEC Standards - Guidance for Industry and Food and Drug Administration Staff
- Premarket Notification [510(k)] Submissions for Ultrasonic Diathermy Devices - Guidance for Industry and Food and Drug Administration Staff
- Marketing Clearance of Diagnostic Ultrasound Systems and Transducers - Guidance for Industry and Food and Drug Administration Staff
- Assembler's Guide to Diagnostic X-Ray Equipment - Guidance for Industry and Food and Drug Administration Staff
- Performance Standard for Diagnostic X-Ray Systems and Their Major Components (21CFR 1020.30, 1020.31, 1020.32, 1020.33); Small Entity Compliance Guide - Guidance for Industry and Food and Drug Administration Staff
- Medical X-ray Imaging (Updated)
- Does the Product Emit Radiation? (Updated)
- Fluoroscopy (Updated)
February 17, 2023
- Updated Emergency Use Authorization
- Network of Experts Program: Connecting the FDA with External Expertise (Updated)
- Federal Register: Premarket Notification Procedures
- Federal Register: Accuracy Requirements for Indication of Temporal-Maximum Ultrasonic Power; Withdrawal
February 16, 2023
- Revised Emergency Use Authorizations
- Revoked Emergency Use Authorizations
- SARS-CoV-2 NGS Assay (Twist Bioscience Corporation)
- Babson Diagnostics aC19G1 (Babson Diagnostics, Inc.)
February 15, 2023
- Revised Emergency Use Authorizations
- Aptima SARS-CoV-2/Flu assay (Hologic, Inc.)
- Fosun COVID-19 RT-PCR Detection Kit (Fosun Pharma USA Inc.)
- Reissued Emergency Use Authorizations
- For consumer information: Prodigy, Proclaim, and Proclaim XR Spinal Cord Stimulation (SCS) Systems - P010032/S189 (Abbott Medical)
- Class I Recall: GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients
February 14, 2023
- Revised Emergency Use Authorization
- List of Cleared or Approved Companion Diagnostic Devices (In Vitro and Imaging Tools) (Updated)
February 13, 2023
- Notifications and Emergency Use Authorizations: FAQs on Testing for SARS-CoV-2 (Updated)
- Nucleic Acid Based Tests (Updated)
- Federal Register: Medical Device Labeling Requirements; Unique Device Identification
February 9, 2023
- Updated Emergency Use Authorization
- Medical Device Material Safety Summaries (Updated)
- Catalog of Regulatory Science Tools to Help Assess New Medical Devices (Updated)
- Extended Expiration Date: CareStart COVID-19 Antigen Home Test and On/go COVID-19 Self-Test
- Personal Protective Equipment EUAs - Appendix A: Authorized Surgical Masks (Updated)
- Update: Certain Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication (Updated)
- FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls (Updated)
February 8, 2023
- New Emergency Use Authorization
- Personal Protective Equipment EUAs - Appendix A: Authorized Surgical Masks (Updated)
- Universal Meditech Inc. Recalls Skippack Medical Lab COVID-19 Direct Antigen Rapid Tests That Are Not Authorized, Cleared, or Approved by the FDA
February 7, 2023
- New Emergency Use Authorizations
- Revised Emergency Use Authorization
- CDRH Petitions (Updated)
- At-Home OTC COVID-19 Diagnostic Tests (Updated)
- Mammography Facility Adverse Event and Action Report – February 7, 2023: Advanced Women Imaging
- Mammography Facilities with Revoked MQSA Certificate (Advanced Women Imaging 02-07-23)
- Updated: Mammography Problems at Advanced Women Imaging in Guttenberg, NJ
February 6, 2023
- Medical Devices Resources for Consumers (Updated)
- Understanding At-Home OTC COVID-19 Antigen Diagnostic Test Results
- Evaluation of Automatic Class III Designation (De Novo) Summaries (DEN220044 added)
February 3, 2023
- Revised Emergency Use Authorization
- 510(k) Third Party Performance Metrics and Accreditation Status (Updated)
February 2, 2023
- Revoked Emergency Use Authorizations
- Advanta Dx SARS-CoV-2 RT-PCR Assay (Standard BioTools Inc.)
- Advanta Dx COVID-19 EASE Assay (Standard BioTools Inc.)
- BinaxNOW COVID-19 Ag 2 Card (Abbott Diagnostics Scarborough, Inc.)
- Evaluation of Automatic Class III Designation (De Novo) Summaries (DEN220014 added)
- Accreditation Scheme for Conformity Assessment (ASCA) 2022 Annual Report
- MedSun Newsletter - February 2023
February 1, 2023
- For Consumer information: FlexAbility Abalation Catheter, Sensor Enabled - P110016/S080 (Abbott Medical)
- CDRH's Experiential Learning Program (Updated)
- Historical Information about Device Emergency Use Authorizations (Updated)
- MQSA National Statistics (Updated)
- Federal Register: Hematology and Pathology Devices; Classification of the Software Algorithm Device to Assist Users in Digital Pathology
January 31, 2023
January 30, 2023
- Class I Recall: Medtronic Recalls Mahurkar Acute Dual Lumen High Flow Hemodialysis Catheters for Potential Catheter Hub Defect
- Surveying, Leveling, and Alignment Laser Products - Guidance for Industry and Food and Drug Administration Staff
- Federal Register: Surveying, Leveling, and Alignment Laser Products
- Federal Register: Cardiovascular Devices; Classification of the Software for Optical Camera-Based Measurement of Pulse Rate, Heart Rate, Breathing Rate, and/or Respiratory Rate
January 27, 2023
- Monkeypox (mpox) and Medical Devices (Updated)
- Health Canada and FDA eSTAR Pilot (Updated)
- Class I Recall: LivaNova (TandemLife) Adds to Recall for LifeSPARC System that May Experience Unintentional Extended Pump Stops Due to Controller Critical Failure
- Federal Register: Premarket Approval of Medical Devices
January 26, 2023
- CDRH 2022 Annual Report
- Class I Recall: Emergent Recalls Certain RSDL (Reactive Skin Decontamination Lotion) Kits Due to Leak Potential
January 25, 2023
- GUDID Data Trends (Updated)
- Class I Recall: Datascope/Getinge Recalls Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps (IABP) for Risk That Blood May Enter Pump Through Damaged Balloon Catheter, Causing Patient Harm
January 24, 2023
- Reissued Emergency Use Authorizations
- Revised Emergency Use Authorizations
- CareStart COVID-19 Antigen Test (Access Bio, Inc.)
- InteliSwab COVID-19 Rapid Test Pro (OraSure Technologies, Inc.)
- Celltrion DiaTrust COVID-19 Ag Home Test (Celltrion USA, Inc.)
- Celltrion DiaTrust COVID-19 Ag Rapid Test (Celltrion USA, Inc.)
- Speedy Swab Rapid COVID-19 Antigen Self-Test (Watmind USA)
- cobas SARS-CoV-2 & Influenza A/B (Roche Molecular Systems, Inc.)
- CDRH Petitions (Updated)
- At-Home OTC COVID-19 Diagnostic Tests (Updated)
- For Consumer information: Agilent Resolution CtDX FIRST - P210040
- Transcript: October 26-27, 2022 General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee Meeting
January 23, 2023
January 20, 2023
- Medtronic HeartWare Ventricular Assist Device (HVAD) System (Updated)
- Recalls Related to the HVAD System (Updated)
January 19, 2023
- At-Home OTC COVID-19 Diagnostic Tests (Updated)
- CDRH Learn (Updated)
- Presentation, Transcript and Printable Slides: Virtual Town Hall Series - Test Development and Validation During Public Health Emergencies Monkeypox (mpox) and COVID-19 - January 11, 2023
- Federal Register: Gastroenterology-Urology Devices; Classification of the Computerized Behavioral Therapy Device for Treating Symptoms of Gastrointestinal Conditions
- Federal Register: Ophthalmic Devices; Classification of the Intense Pulsed Light Device for Managing Dry Eye
- Federal Register: Records and Reports for Radiation Emitting Electronic Products; Performance Standards for Diagnostic X-ray, Laser, and Ultrasonic Products
January 18, 2023
- FDA Seeks Public Comment: Advancing Real-World Data and Real-World Evidence with User Fee Funding (MDUFA V)
- Federal Register: Adverse Event Program for Medical Devices (Medical Product Safety Network)
January 17, 2023
- Reissued Emergency Use Authorizations
- Updated Emergency Use Authorization
January 13, 2023
- ASCA-Recognized Accreditation Bodies (Updated)
- At-Home OTC COVID-19 Diagnostic Tests (Updated)
- Federal Register: Clinical Chemistry and Clinical Toxicology Devices; Classification of the Prognostic Test for Assessment of Liver Related Disease Progression
January 12, 2023
- New Emergency Use Authorization
- Revised Emergency Use Authorizations
- Webinar: Electromagnetic Compatibility (EMC) of In Vitro Diagnostic Devices, February 2, 2023
- Policy for Coronavirus Disease-2019 Tests (Revised) - Guidance for Developers and Food and Drug Administration Staff
- Policy for Evaluating Impact of Viral Mutations on COVID-19 Tests (Revised) - Guidance for Test Developers and Food and Drug Administration Staff
- Hearing Aids (Updated)
- Federal Register: Neurological Devices; Classification of the Digital Therapy Device to Reduce Sleep Disturbance for Psychiatric Conditions
January 11, 2023
- New Emergency Use Authorization
- Updated Emergency Use Authorizations
- Photobiomodulation (PBM) Devices - Premarket Notification [510(k)] Submissions - Draft Guidance for Industry and Food and Drug Administration Staff
- Federal Register: Photobiomodulation Devices--Premarket Notification Submissions
January 5, 2023
- Revoked Emergency Use Authorization
- Federal Register: Cardiovascular Devices: Classification of the Hardware and Software for Optical Camera-Based Measurement of Pulse Rate, Heart Rate, Breathing Rate, and/or Respiratory Rate
- Federal Register: Ear, Nose, and Throat Devices: Classification of the Powered Insertion System for a Cochlear Implant Electrode Array
- Federal Register: Orthopedic Devices: Classification of the Resorbable Shoulder Spacer
- Federal Register: Physical Medicine Devices: Classification of the Electroencephalography-Driven Upper Extremity Powered Exerciser
- Federal Register: Physical Medicine Devices: Classification of the Virtual Reality Behavioral Therapy Device for Pain Relief
January 4, 2023
- Federal Register: Neurological Devices; Classification of the Brain Stimulation Programming Planning Software
- Federal Register: Orthopedic Devices; Classification of the Bone Indentation Device
- Federal Register: Orthopedic Devices; Classification of the Implantable Post-Surgical Kinematic Measurement Knee Device
January 3, 2023
- MQSA National Statistics (Updated)