Nipro Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE, NIPRO SAFETOUCH HUBER INFUSTION SET, NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nipro Medical Corp. Cardiovascular ✕
2 devices