Telemed Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PPD BALLOON DILATATION CATHETER, MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOON, FLEXIBLE ENDOSCOPIC SCISSORS
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Telemed Systems, Inc. General Hospital ✕
1 devices