Medical Device Manufacturer · US , Marlton , NJ

Mid-Atlantic Diagnostics, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000

Total

Cleared

Denied

Mid-Atlantic Diagnostics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Marlton, US.

Historical record: 4 cleared submissions from 2000 to 2010. Primary specialty: Obstetrics & Gynecology.

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

Mid-Atlantic Diagnostics, Inc. is one of 23726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mid-Atlantic Diagnostics, Inc.

4 devices

1-4 of 4