FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NIPRO DISPOSABLE SYRINGE

K Number: K091279 · Decision Aug 12, 2009
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
34
Review Days
103

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Basic Information

Device Name
NIPRO DISPOSABLE SYRINGE
K Number
K091279
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nipro Medical Corporation
Date Received
May 1, 2009
Decision Date
August 12, 2009
Product Code
FMF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMF Syringe, Piston

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K Number Device Name
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K190037 Cronus HP PTA Balloon Catheter
K191359 Nipro Syringe
K182940 Surdial DX Hemodialysis System
K173029 Nipro Syringe
K161681 Nipro SafeTouch IV Catheter
K160444 FB-U Hemodialyzer
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