Medical Device Manufacturer · US , Cambridge , MA

Intracel Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Intracel Corp. has 5 FDA 510(k) cleared medical devices. Based in Cambridge, US.

Historical record: 5 cleared submissions from 1995 to 2000. Primary specialty: Microbiology.

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

Intracel 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 - Intracel Corp.

5 devices

1-5 of 5