Medical Device Manufacturer · US , Duarte , CA

Catalina Biomedical Corp. - FDA 510(k) Cleared Devices

5 submissions · 3 cleared · Since 1990

Total

Cleared

Denied

Catalina Biomedical Corp. has 3 FDA 510(k) cleared medical devices. Based in Duarte, US.

Historical record: 3 cleared submissions from 1990 to 1992. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Catalina Biomedical Corp. Filter by specialty or product code using the sidebar.

Catalina Biomedical Corp. 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 - Catalina Biomedical Corp.

5 devices

1-5 of 5