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

VICKERS ERGOMATIC MICROS INSTR-FINE R OR L HANDED

K Number: K853181 · Decision Oct 28, 1985
Classifications
1
FEI Numbers
145
Registration Numbers
145
Same Product Code
12
Applicant Total
59
Review Days
90

Basic Information

Device Name
VICKERS ERGOMATIC MICROS INSTR-FINE R OR L HANDED
K Number
K853181
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4525
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
KEELER INSTRUMENTS, INC.
Date Received
July 30, 1985
Decision Date
October 28, 1985
Product Code
GZX
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GZX Instrument, Microsurgical

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