510(k) K093451

Device
OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP
Applicant
OMNIGUIDE, INC.
510(k) number
K093451
Product code
GEX  
Decision
Substantially Equivalent (SESE)
Decision date
2009-11-20
Date received
2009-11-05
Regulation
878.4810
Classification name
Powered Laser Surgical Instrument
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Applicant Contact#

Contact
DOUGLAS W WOODRUFF
Address
One Kendall Sq., Bldg. 100 3rd Floor Cambridge MA US 02139 02139

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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Legacy Summary#

summary

FDA Review#

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