Nipro Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Nipro Medical Corp. has 27 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 27 cleared submissions from 1997 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nipro Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nipro Medical Corp.
27 devices
Cleared
Jan 22, 2010
NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE
Gastroenterology & Urology
29d
Cleared
Oct 21, 2008
NIPRO SAFETOUCH HUBER INFUSTION SET
General Hospital
175d
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
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