Pauline M. Nicholls is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pauline M. Nicholls - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pauline M. Nicholls has 1 FDA 510(k) cleared medical devices. Based in Monroe, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pauline M. Nicholls Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pauline M. Nicholls
1 devices