A&M Technology is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
A&M Technology - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
A&M Technology has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by A&M Technology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A&M Technology
1 devices