K-number	K111441
Device name	UNIMAX VERESS NEEDLE
Applicant	Unimax Medical Systems, Inc.
Product code	HIF
Device class	Class II
Decision date	Aug 19, 2011
Decision	Substantially Equivalent
Regulation	884.1730

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Source

View the full FDA submission: accessdata.fda.gov

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UNIMAX VERESS NEEDLE

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