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FDA 510(k)

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

K-Number: K173262 · 2018-03-06

Decision Date2018-03-06
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is a medical device manufactured by Innovative Health, LLC. It received FDA 510(k) clearance on 2018-03-06 under approval number K173262. The device is classified under product code OWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is a medical device that received FDA 510(k) clearance on 2018-03-06. It is manufactured by Innovative Health, LLC. The 510(k) number is K173262.

When was Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter approved by the FDA?

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter received FDA 510(k) clearance on 2018-03-06, under approval number K173262.

What company makes Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is manufactured by Innovative Health, LLC.

What is the FDA product code for Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter?

The FDA product code for Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter is OWQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.