K-number	K982399
Device name	DISETRONIC PENFINE INJECTION PEN NEEDLE
Applicant	Disetronic Medical Systems
Product code	FMI
Device class	Class II
Decision date	Aug 6, 1998
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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DISETRONIC PENFINE INJECTION PEN NEEDLE

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