K-number	K875240
Device name	TRANS/V NEEDLE GUIDE
Applicant	CIVCO Medical Instruments Co., Inc.
Product code	IYO
Device class	Class II
Decision date	Apr 15, 1988
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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TRANS/V NEEDLE GUIDE

Everything you need for a 510(k) submission. Nothing you don't.