K-number	K160235
Device name	ViaValve Safety I.V. Catheter
Applicant	Smiths Medical Asd, Inc.
Product code	FOZ
Device class	Class II
Decision date	Jun 30, 2016
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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ViaValve Safety I.V. Catheter

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