Medical Device Manufacturer · US , Scarsdale , NY

Mark H. Friedman - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Mark H. Friedman has 2 FDA 510(k) cleared medical devices. Based in Scarsdale, US.

Historical record: 2 cleared submissions from 1996 to 2004. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Mark H. Friedman Filter by specialty or product code using the sidebar.

Mark H. Friedman 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 - Mark H. Friedman

2 devices

1-2 of 2