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

LQ1106 OPHTHALMIC YAG LASER

K Number: K882772 · Decision Aug 26, 1988
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
59
Review Days
51

Basic Information

Device Name
LQ1106 OPHTHALMIC YAG LASER
K Number
K882772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
KEELER INSTRUMENTS, INC.
Date Received
July 6, 1988
Decision Date
August 26, 1988
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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