Medical Device Manufacturer · US , Glens Falls , NY

Schneider/Namic - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1998

Total

Cleared

Denied

Schneider/Namic has 1 FDA 510(k) cleared medical devices. Based in Glens Falls, US.

Historical record: 1 cleared submissions from 1998 to 1999. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Schneider/Namic Filter by specialty or product code using the sidebar.

Schneider/Namic 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 - Schneider/Namic

2 devices

1-2 of 2