Medical Device Manufacturer · US , Chattanooga , TN

Intera Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

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

Historical record: 6 cleared submissions from 1986 to 1989. Primary specialty: Gastroenterology & Urology.

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

Intera 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 - Intera Corp.

6 devices

1-6 of 6