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

ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY

K Number: K912968 · Decision Sep 25, 1991
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
1
Review Days
79

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Basic Information

Device Name
ELEC SURG INSTR FOR LOPPROSCOPE CHOLECYSTECYOMY
K Number
K912968
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
Paden Foudry , Ltd.
Date Received
July 8, 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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