Medical Device Manufacturer · US , Irvine , CA

Cytocare, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1992

Total

Cleared

Denied

Cytocare, Inc. has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 7 cleared submissions from 1992 to 1995. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Cytocare, Inc. Filter by specialty or product code using the sidebar.

Cytocare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cytocare, Inc.

7 devices

1-7 of 7