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

ALLOY SCALPEL HANDPIECES

K Number: K914197 · Decision Apr 10, 1992
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
13
Review Days
204

Basic Information

Device Name
ALLOY SCALPEL HANDPIECES
K Number
K914197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
LASER, INC.
Date Received
September 19, 1991
Decision Date
April 10, 1992
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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