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

SURGILASE YAG 100 SURGICAL LASER SYSTEM

K Number: K902211 · Decision Jun 29, 1990
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
19
Review Days
50

Basic Information

Device Name
SURGILASE YAG 100 SURGICAL LASER SYSTEM
K Number
K902211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
SURGILASE, INC.
Date Received
May 10, 1990
Decision Date
June 29, 1990
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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K Number Device Name
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K905006 SURGILASE SL 150 SURGICAL LASER SYSTEM
K904203 SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEM
K900570 SURGILASE YAG 100 IN ORTHOPEDIC SURGERY
K901211 SURGILASE SL50 SURGICAL LASER SYSTEM
K901227 SURGILASE CO2 SURGICAL LASER SYSTEMS MODEL SL120
K894471 SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY
K894396 SURGILASE 25, 40, 45, 55, 60, 80, 100 LASER
K891461 SURGILASE YAG 100 SURGICAL ND:YAG LASER/GEN SURG
Search all 19 clearances from SURGILASE, INC. →