Nipro Medical Corp. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nipro Medical Corp. Gastroenterology & Urology ✕
9 devices
Cleared
Jan 22, 2010
NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE
Gastroenterology & Urology
29d
Cleared
Oct 04, 2007
NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL...
Gastroenterology & Urology
72d
Cleared
Feb 05, 2007
NIPRO BIOHOLE NEEDLE
Gastroenterology & Urology
90d
Cleared
Jan 12, 2007
NIPRO SAFETOUCH II GAMMA
Gastroenterology & Urology
28d
Cleared
Apr 27, 2001
NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND...
Gastroenterology & Urology
88d
Cleared
Dec 05, 2000
NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND...
Gastroenterology & Urology
209d
Cleared
Nov 21, 2000
NIPRO SAFETOUCH SAFETY FISTULA NEEDLE
Gastroenterology & Urology
74d
Cleared
Aug 09, 1999
NIPRO ARTERIAL VENOUS FISTULA NEEDLE, AGULHA PARA FISTULA ARTERIO-VENOSA,...
Gastroenterology & Urology
90d
Cleared
Nov 26, 1997
NIPRO BLOOD TUBING SET WITH TRANSDUCER AND SOLUTION SET FOR HEMODIALYSIS
Gastroenterology & Urology
168d