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Nipro Medical Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K093985NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLEJanuary 22, 2010
K081210NIPRO SAFETOUCH HUBER INFUSTION SETOctober 21, 2008
K072024NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634October 4, 2007
K063368NIPRO BIOHOLE NEEDLEFebruary 5, 2007
K063721NIPRO SAFETOUCH II GAMMAJanuary 12, 2007
K052474NIPRO HYPODERMIC NEEDLENovember 10, 2005
K051574NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLEAugust 26, 2005
K041779NIPRO DISPOSABLE STOPCOCKS, MODELS 3W-RC. NCN-3, 3W-R, 3W-LSeptember 21, 2004
K032777MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLENovember 14, 2003
K030683NIPRO DISPOSABLE SYRINGESOctober 31, 2003
K022756NIPRO BIO-FLEX CATHETEROctober 18, 2002
K013293NIPRO HYPODERMIC NEEDLEDecember 14, 2001
K013287NIPRO SAFELET CATHDecember 3, 2001
K011297NIPRO SAFETOUCH SCALP VEIN AND BLOOD COLLECTION SETJune 20, 2001
K010264NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SETApril 27, 2001
K003394APPALEAD GW+03XXXXXXR SERIESJanuary 30, 2001
K001465NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SETDecember 5, 2000
K002813NIPRO SAFETOUCH SAFETY FISTULA NEEDLENovember 21, 2000
K001251SNIPER, MODEL OR-3872XX SERIESJuly 7, 2000
K992699NIPRO BLOOD COLLECTION NEEDLEFebruary 14, 2000