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

IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003

K Number: K912229 · Decision Sep 25, 1991
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
56
Review Days
128

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Basic Information

Device Name
IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
K Number
K912229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dlp, Inc.
Date Received
May 20, 1991
Decision Date
September 25, 1991
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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