Medical Device Manufacturer · US , Atlanta , GA

D.L. Nelson and Assoc., Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990

Total

Cleared

Denied

D.L. Nelson and Assoc., Inc. has 4 FDA 510(k) cleared medical devices. Based in Atlanta, US.

Historical record: 4 cleared submissions from 1990 to 1995. Primary specialty: General & Plastic Surgery.

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

D.L. Nelson and 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 - D.L. Nelson and Assoc., Inc.

4 devices

1-4 of 4