Meadox Surgimed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MS CLASSIQUE BALLOON CATHETER, NOPROFILE OLBERT CATHETER SYSTEM, MS AMPLATZ EXTRA STIFF GUIDE WIRE
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meadox Surgimed, Inc. General Hospital ✕
2 devices