K-number	K830568
Device name	GUTTMAN INFUSION NEEDLE
Applicant	Cosmetic Sciences, Inc.
Product code	FMI
Device class	Class II
Decision date	Oct 27, 1983
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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GUTTMAN INFUSION NEEDLE

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