K-number	K010958
Device name	FISTULOK FISTULA NEEDLE PROTECTION
Applicant	Diasol, Inc.
Product code	FMI
Device class	Class II
Decision date	May 18, 2001
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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FISTULOK FISTULA NEEDLE PROTECTION

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