K-number	K173262
Device name	Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter
Applicant	Innovative Health, LLC
Product code	OWQ
Device class	Class II
Decision date	Mar 6, 2018
Decision	Substantially Equivalent
Regulation	870.1200

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Source

View the full FDA submission: accessdata.fda.gov

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Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

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