K-number	K945461
Device name	PITON(TM) Y-PACK AND PITON(TM) TRI-PACK)
Applicant	Medtronics Interventional Vascular
Product code	DTL
Device class	Class II
Decision date	Feb 3, 1995
Decision	Substantially Equivalent
Regulation	870.4290

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View the full FDA submission: accessdata.fda.gov

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PITON(TM) Y-PACK AND PITON(TM) TRI-PACK)

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