FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SURGIMOTOR

K Number: K954470 · Decision Dec 8, 1995
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
40
Applicant Total
26
Review Days
73

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Basic Information

Device Name
SURGIMOTOR
K Number
K954470
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
W.O.M. World of Medicine GmbH
Date Received
September 26, 1995
Decision Date
December 8, 1995
Product Code
GEY
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
GEY Motor, Surgical Instrument, Ac-Powered

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