Plastimed Laboratoire Pharmaceutique is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plastimed Laboratoire Pharmaceutique - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Plastimed Laboratoire Pharmaceutique has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 1998 to 2000. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Plastimed Laboratoire Pharmaceutique Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Plastimed Laboratoire Pharmaceutique
2 devices