FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

U&U Blood Collection Sets

K Number: K181508 · Decision Feb 13, 2019
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
10
Review Days
251

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Basic Information

Device Name
U&U Blood Collection Sets
K Number
K181508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
U&U Medical Technology Co, Ltd.
Date Received
June 7, 2018
Decision Date
February 13, 2019
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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K Number Device Name
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K151151 U & U Intravascular Administration Set
K143637 U&U Sterilization Pouch and Roll
K143629 U&U Bowie-Dick Test Pack
K132553 U&U STERILE PISTON SYRINGE WITHOUT NEEDLE
K123162 U&U HYDROGEN PEROXIDE GAS PLASMA STERILIZATION POUCH/ROLL
K132552 U&U STERILE HYPODERMIC NEEDLE