K-number	K992653
Device name	SHELLY PROTECTED AV FISTULA NEEDLE
Applicant	Diasol, Inc.
Product code	FIE
Device class	Class II
Decision date	Oct 27, 1999
Decision	Substantially Equivalent
Regulation	876.5540

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Source

View the full FDA submission: accessdata.fda.gov

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SHELLY PROTECTED AV FISTULA NEEDLE

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