• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
1 to 10 of 10 Results
ProductCode: GEX Applicant: OMNIGUIDE, INC Decision Date To: 09/23/2014
Results per Page
New Search
Export all 10 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
omniguide beampath co2 mark iii waveguid omniguide, inc. K093451 11/20/2009
omniguide beampath fels 25a co2 laser sy omniguide, inc. K093251 10/29/2009
omniguide beampath fiber optic handpiece omniguide, inc. K081939 08/12/2008
mark iii waveguide fiber with low profil omniguide, inc. K073313 01/02/2008
omniguide sterile waveguide adapter syst omniguide, inc. K073409 12/14/2007
omniguide beam path co2 mark iii wavegui omniguide, inc. K070157 02/01/2007
omniguide zero flow zf-t waveguide fiber omniguide, inc. K070071 01/25/2007
omniguide zero flow zf-t 150 waveguide f omniguide, inc. K063141 11/29/2006
omniguide beampath laser beam delivery s omniguide, inc. K062423 09/21/2006
highland beam delivery system, model 3-0 omniguide, inc. K061909 07/19/2006
-
-