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

DESERET CAPACITY PLUS ELECTROSURG. PAD

K Number: K821356 · Decision Jul 14, 1982
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
50
Review Days
69

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Basic Information

Device Name
DESERET CAPACITY PLUS ELECTROSURG. PAD
K Number
K821356
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Warner-Lambert Co.
Date Received
May 6, 1982
Decision Date
July 14, 1982
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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