Medical Device Manufacturer · US , Garden City , NY

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

7 submissions · 7 cleared · Since 1994

Total

Cleared

Denied

Univec, Inc. has 7 FDA 510(k) cleared medical devices. Based in Garden City, US.

Historical record: 7 cleared submissions from 1994 to 2002. Primary specialty: General Hospital.

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

Univec, 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 - Univec, Inc.

7 devices

1-7 of 7