Monkeypox and Medical Devices
The FDA issued a policy for monkeypox tests to address the public health emergency.
The FDA issued a policy for monkeypox tests to address the public health emergency.
Find answers to frequently asked questions on Philips Respironics ventilators, BiPAP, and CPAP machines recall.
This action enables consumers with perceived mild to moderate hearing impairment to purchase hearing aids from retailers without the need for a medical exam, prescription, or a fitting.
The FDA recommends repeat testing following a negative result whether or not you have COVID-19 symptoms.
List of authorized at-home OTC COVID-19 diagnostic tests and expiration date information.
FDA issued a safety communication to use and store at-home COVID-19 tests properly to avoid potential harm.
Information and news on device recalls, other safety issues, approvals, and other device and radiation-emitting product topics.