North American Instrument Corp. - FDA 510(k) Cleared Devices
Recent clearances: SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS), HEMO-VALVE, EPIC INTRODUCER SHEATH
28
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - North American Instrument Corp. Gastroenterology & Urology ✕
1 devices