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

SINGLE USE GROUNDING PAD

K Number: K132136 · Decision Sep 6, 2013
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
5
Review Days
57

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Basic Information

Device Name
SINGLE USE GROUNDING PAD
K Number
K132136
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lccs Products Limited
Date Received
July 11, 2013
Decision Date
September 6, 2013
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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