The Saunders Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Saunders Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
The Saunders Group has 2 FDA 510(k) cleared medical devices. Based in Chaska, US.
Historical record: 2 cleared submissions from 1994 to 2000. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by The Saunders Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Saunders Group
2 devices