Medical Device Manufacturer · US , Brewerton , NY

Nasiff Assoc., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Nasiff Assoc., Inc. has 5 FDA 510(k) cleared medical devices. Based in Brewerton, US.

Historical record: 5 cleared submissions from 1990 to 2000. Primary specialty: Cardiovascular.

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

Nasiff Assoc., 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 - Nasiff Assoc., Inc.

5 devices

1-5 of 5