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

OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP

K Number: K093451 · Decision Nov 20, 2009
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
11
Review Days
15

Basic Information

Device Name
OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP
K Number
K093451
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OMNIGUIDE, INC.
Date Received
November 5, 2009
Decision Date
November 20, 2009
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
Y

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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Other Clearances by OMNIGUIDE, INC.

K Number Device Name
K140378 FLEXGUIDE ULTRA BEAMPATH ROBOTIC FIBER CONDUIT
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K081939 OMNIGUIDE BEAMPATH FIBER OPTIC HANDPIECE SYSTEM AND STERILIZATION TRAY
K073313 MARK III WAVEGUIDE FIBER WITH LOW PROFILE TIP
K073409 OMNIGUIDE STERILE WAVEGUIDE ADAPTER SYSTEM
K070157 OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER
K070071 OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER
K063141 OMNIGUIDE ZERO FLOW ZF-T 150 WAVEGUIDE FIBER
K062423 OMNIGUIDE BEAMPATH LASER BEAM DELIVERY SYSTEM
K061909 HIGHLAND BEAM DELIVERY SYSTEM, MODEL 3-099-002-00-00
Search all 11 clearances from OMNIGUIDE, INC. →