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

GYNEGUIDE

K Number: K894591 · Decision Oct 10, 1989
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
28
Review Days
78

Basic Information

Device Name
GYNEGUIDE
K Number
K894591
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
MARLO SURGICAL TECHNOLOGY
Date Received
July 24, 1989
Decision Date
October 10, 1989
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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