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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