Medical Device Manufacturer · US , San Diego , CA

Cytori Therapeutics, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2006

Recent clearances: PUREGRAFT 50 SYSTEM, PUREGRAFT 850/PURE SYSTEM, CYTORI PUREGRAFT 250/PURE SYSTEM

6
Total
6
Cleared
0
Denied

FDA 510(k) Regulatory Record - Cytori Therapeutics, Inc. Anesthesiology ✕

1 devices
1-1 of 1
Filters