The Anthros Medical Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Anthros Medical Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
The Anthros Medical Group has 2 FDA 510(k) cleared medical devices. Based in Highland, US.
Historical record: 2 cleared submissions from 1992 to 1994. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by The Anthros Medical Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Anthros Medical Group
2 devices