Medical Device Manufacturer · US , Washington , DC

The Dezac Group - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2002

Total

Cleared

Denied

The Dezac Group has 3 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 3 cleared submissions from 2002 to 2002. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by The Dezac Group Filter by specialty or product code using the sidebar.

The Dezac Group 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 - The Dezac Group

3 devices

1-3 of 3