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Medisurg , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K063468
THE FUGO BLADE FOR DENTISTRY
April 18, 2007
K050933
FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300
December 9, 2005
K041019
THE FUGO BLADE FOR GLAUCOMA
October 8, 2004
K001498
THE FUGO BLADE
August 10, 2000