Andover Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CANMED 451, NORTECH MODEL 86901000 ELECTRODE, MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Andover Medical, Inc. Neurology ✕
3 devices