Conmed Endoscopic Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998, CONMED AXCESS PAPILLOTOME MODELS AX4535, AX4535FX
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Conmed Endoscopic Technologies, Inc. Gastroenterology & Urology ✕
2 devices