BK220693 - PUREGRAFT 850/PURE SYSTEM
510(k) Number: BK220693
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 850/PURE SYSTEM
Decision Date: 3/7/2012
510(k) Number: BK220693
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 850/PURE SYSTEM
Decision Date: 3/7/2012