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

Small Foam Kit, Medium Foam Kit, Large Foam Kit, Extra Large Foam Kit

K Number: K211571 · Decision May 31, 2022
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
204
Applicant Total
3
Review Days
375

Basic Information

Device Name
Small Foam Kit, Medium Foam Kit, Large Foam Kit, Extra Large Foam Kit
K Number
K211571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zhejiang Longterm Medical Technology Co., LTD
Date Received
May 21, 2021
Decision Date
May 31, 2022
Product Code
OMP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
OMP Negative Pressure Wound Therapy Powered Suction Pump

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