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

OPTILITE (TM) FIBEROPTIC DELIVERY SYSTEMS AND ACCE

K Number: K910114 · Decision Apr 9, 1991
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
26
Review Days
89

Basic Information

Device Name
OPTILITE (TM) FIBEROPTIC DELIVERY SYSTEMS AND ACCE
K Number
K910114
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
XINTEC CORPORATION
Date Received
January 10, 1991
Decision Date
April 9, 1991
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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K981350 ALEXIS ALEXANDRITE LASER SYSTEM AND ACCESSORIES
K971912 PROTEGE ER:YAG LASER SYSTEM AND ACCESSORIES
K971065 DENTICA PULSED ND: YAG LASER SYSTEMS AND ACCESSORIES
K951935 PRODIGY SUPERPULSE ND:YAG SURGICAL LASER SYSTEMS & ACCESSORIES
K951876 PROTEGE ER:YAG SURGICAL LASER SYSTEM AND ACCESSORIES
K951910 ODYSSEY HO:YAG SURGICAL LASER SYSTEMS & ACCESSORIES
K951760 OPTILITE VIII LASER SURGERY ACCESSORIES
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