Medical Device Manufacturer · US , Stamford , CT

Circon Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1997

Total

Cleared

Denied

Circon Corp. has 6 FDA 510(k) cleared medical devices. Based in Stamford, US.

Historical record: 6 cleared submissions from 1997 to 1999. Primary specialty: Obstetrics & Gynecology.

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

Circon 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 - Circon Corp.

6 devices

1-6 of 6