Endochoice, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Fuse Endoscopic System with FuseBox Processor, EndoChoice Water Bottle Cap Irrigation System, Seal Single-Use Biopsy Valve
27
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Endochoice, Inc. Anesthesiology ✕
1 devices