Medical Device Manufacturer · US , Fort Lauderdale , FL

Gmp/Companies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

Gmp/Companies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.

Historical record: 2 cleared submissions from 2003 to 2005. Primary specialty: Cardiovascular.

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

Gmp/Companies, 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 - Gmp/Companies, Inc.

2 devices

1-2 of 2