Amplus Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amplus Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Amplus Corp. has 4 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 4 cleared submissions from 1988 to 1990. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Amplus Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amplus Corp.
4 devices