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FDA 510(k)

Reprocessed Electrophysiology Catheter

K-Number: K153153 · 2016-03-14

Decision Date2016-03-14
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed Electrophysiology Catheter is a medical device manufactured by Innovative Health, LLC. It received FDA 510(k) clearance on 2016-03-14 under approval number K153153. The device is classified under product code NLH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed Electrophysiology Catheter?

Reprocessed Electrophysiology Catheter is a medical device that received FDA 510(k) clearance on 2016-03-14. It is manufactured by Innovative Health, LLC. The 510(k) number is K153153.

When was Reprocessed Electrophysiology Catheter approved by the FDA?

Reprocessed Electrophysiology Catheter received FDA 510(k) clearance on 2016-03-14, under approval number K153153.

What company makes Reprocessed Electrophysiology Catheter?

Reprocessed Electrophysiology Catheter is manufactured by Innovative Health, LLC.

What is the FDA product code for Reprocessed Electrophysiology Catheter?

The FDA product code for Reprocessed Electrophysiology Catheter is NLH.

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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.