Nissho Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nissho Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Nissho Corp. has 5 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 5 cleared submissions from 1994 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nissho Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nissho Corp.
5 devices
Cleared
Mar 04, 1997
NIPRO ARTERIAL & VENOUS BLOOD TUBING SET FOR HEMODIALYSIS
Gastroenterology & Urology
511d
Cleared
Jun 04, 1996
NIPRO ARTERIAL VENOUS FISTULA NEEDLE
Gastroenterology & Urology
204d
Cleared
Mar 28, 1996
NIPRO SAFELET CATH
General Hospital
84d
Cleared
Jan 04, 1996
NIPRO SCALP VEIN SET (DISPOSABL PSV SET)
General Hospital
59d
Cleared
Dec 07, 1994
NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES
General Hospital
91d