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

U&U HYDROGEN PEROXIDE GAS PLASMA STERILIZATION POUCH/ROLL

K Number: K123162 · Decision Feb 26, 2014
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
10
Review Days
505

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
U&U HYDROGEN PEROXIDE GAS PLASMA STERILIZATION POUCH/ROLL
K Number
K123162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
U&U Medical Technology Co, Ltd.
Date Received
October 9, 2012
Decision Date
February 26, 2014
Product Code
FRG
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
FRG Wrap, Sterilization

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FRG), ordered by most recent decision date.

View all

Other Clearances by U&U Medical Technology Co, Ltd.

K Number Device Name
K181508 U&U Blood Collection Sets
K171823 U&U Indicator tape and strip
K160855 U&U Enteral Syringe
K152808 U&U Insulin Syringe with/without Safety Retractable Device
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
K132552 U&U STERILE HYPODERMIC NEEDLE