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FDA 510(k)

Reprocessed Diagnostic Ultrasound Catheter

K-Number: K153090 · 2016-03-10

Decision Date2016-03-10
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed Diagnostic Ultrasound Catheter is a medical device manufactured by Innovative Health, LLC. It received FDA 510(k) clearance on 2016-03-10 under approval number K153090. 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 Diagnostic Ultrasound Catheter?

Reprocessed Diagnostic Ultrasound Catheter is a medical device that received FDA 510(k) clearance on 2016-03-10. It is manufactured by Innovative Health, LLC. The 510(k) number is K153090.

When was Reprocessed Diagnostic Ultrasound Catheter approved by the FDA?

Reprocessed Diagnostic Ultrasound Catheter received FDA 510(k) clearance on 2016-03-10, under approval number K153090.

What company makes Reprocessed Diagnostic Ultrasound Catheter?

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

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

The FDA product code for Reprocessed 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.