Medical Device Manufacturer · US , Thorofare , NJ

Akers Laboratories, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2003

Total

Cleared

Denied

Akers Laboratories, Inc. has 3 FDA 510(k) cleared medical devices. Based in Thorofare, US.

Historical record: 3 cleared submissions from 2003 to 2004.

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

Akers Laboratories, 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 - Akers Laboratories, Inc.

3 devices

1-3 of 3