K-number	K002813
Device name	NIPRO SAFETOUCH SAFETY FISTULA NEEDLE
Applicant	Nipro Medical Corp.
Product code	FIE
Device class	Class II
Decision date	Nov 21, 2000
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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NIPRO SAFETOUCH SAFETY FISTULA NEEDLE

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