Nipro Medical Corp. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nipro Medical Corp. General Hospital ✕
16 devices
Cleared
Oct 21, 2008
NIPRO SAFETOUCH HUBER INFUSTION SET
General Hospital
175d
Cleared
Nov 10, 2005
NIPRO HYPODERMIC NEEDLE
General Hospital
62d
Cleared
Aug 26, 2005
NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE
General Hospital
73d
Cleared
Sep 21, 2004
NIPRO DISPOSABLE STOPCOCKS, MODELS 3W-RC. NCN-3, 3W-R, 3W-L
General Hospital
82d
Cleared
Nov 14, 2003
MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE
General Hospital
67d
Cleared
Oct 31, 2003
NIPRO DISPOSABLE SYRINGES
General Hospital
240d
Cleared
Oct 18, 2002
NIPRO BIO-FLEX CATHETER
General Hospital
59d
Cleared
Dec 14, 2001
NIPRO HYPODERMIC NEEDLE
General Hospital
73d
Cleared
Dec 03, 2001
NIPRO SAFELET CATH
General Hospital
62d
Cleared
Jun 20, 2001
NIPRO SAFETOUCH SCALP VEIN AND BLOOD COLLECTION SET
General Hospital
51d
Cleared
Feb 14, 2000
NIPRO BLOOD COLLECTION NEEDLE
General Hospital
186d
Cleared
Feb 11, 2000
NIPRO INSULIN SYRINGE
General Hospital
24d
Cleared
Jan 13, 2000
NIPRO LUER ADAPTOR
General Hospital
153d
Cleared
Dec 22, 1997
NIPRO CORELESS NEEDLE/CORELESS NEEDLE SET
General Hospital
236d
Cleared
Sep 18, 1997
NIPRO DISPOSABLE SOLUTION INFUSION SET
General Hospital
77d
Cleared
Mar 27, 1997
NIPRO DISPOSABLE SOLUTION INFUSION SET
General Hospital
77d