K-number	K192318
Device name	Ultraverse 014 and 018 PTA Balloon Dilatation Catheters
Applicant	Bard Peripheral Vascular, Inc.
Product code	LIT
Device class	Class II
Decision date	Oct 3, 2019
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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Ultraverse 014 and 018 PTA Balloon Dilatation Catheters

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