Nissho Corp. - FDA 510(k) Cleared Devices
Recent clearances: NIPRO ARTERIAL & VENOUS BLOOD TUBING SET FOR HEMODIALYSIS, NIPRO ARTERIAL VENOUS FISTULA NEEDLE, NIPRO SAFELET CATH
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nissho Corp. General Hospital ✕
3 devices