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FDA 510(k) Applications Submitted by MEDISURG LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050933
04/14/2005
FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300
MEDISURG LTD.
K041019
04/20/2004
THE FUGO BLADE FOR GLAUCOMA
MEDISURG LTD.
K001498
05/15/2000
THE FUGO BLADE
MEDISURG LTD.
K063468
11/16/2006
THE FUGO BLADE FOR DENTISTRY
MEDISURG LTD.
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