K-number	K041019
Device name	THE FUGO BLADE FOR GLAUCOMA
Applicant	Medisurg , Ltd.
Product code	NCR
Device class	Class II
Decision date	Oct 8, 2004
Decision	Substantially Equivalent
Regulation	886.4100

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View the full FDA submission: accessdata.fda.gov

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THE FUGO BLADE FOR GLAUCOMA

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