Medical Device Manufacturer · US , Miami , FL

Nipro Medical Corp. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1997

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

FDA 510(k) Regulatory Record - Nipro Medical Corp. General Hospital ✕

16 devices

1-12 of 16

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