BK220699 - PUREGRAFT 50 SYSTEM
510(k) Number: BK220699
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 50 SYSTEM
Decision Date: 1/24/2014
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK220699
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 50 SYSTEM
Decision Date: 1/24/2014