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FDA 510(k)

Reprocessed Torqr Diagnostic EP Catheter

K-Number: K181618 · 2018-10-18

Decision Date2018-10-18
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed Torqr Diagnostic EP Catheter is a medical device manufactured by Innovative Health, LLC. It received FDA 510(k) clearance on 2018-10-18 under approval number K181618. 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 Torqr Diagnostic EP Catheter?

Reprocessed Torqr Diagnostic EP Catheter is a medical device that received FDA 510(k) clearance on 2018-10-18. It is manufactured by Innovative Health, LLC. The 510(k) number is K181618.

When was Reprocessed Torqr Diagnostic EP Catheter approved by the FDA?

Reprocessed Torqr Diagnostic EP Catheter received FDA 510(k) clearance on 2018-10-18, under approval number K181618.

What company makes Reprocessed Torqr Diagnostic EP Catheter?

Reprocessed Torqr Diagnostic EP Catheter is manufactured by Innovative Health, LLC.

What is the FDA product code for Reprocessed Torqr Diagnostic EP Catheter?

The FDA product code for Reprocessed Torqr Diagnostic EP 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.