United States Endoscopy Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: gi-4000 Electrosurgical Generator, Lariat, Hot/Cold Snare, Bio Guard Air/Water & Suction Valves
94
Total
92
Cleared
0
Denied
FDA 510(k) Regulatory Record - United States Endoscopy Group, Inc. Cardiovascular ✕
2 devices