A.P.Deauville, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A.P.Deauville, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
A.P.Deauville, LLC has 1 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by A.P.Deauville, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A.P.Deauville, LLC
1 devices