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FDA 510(k)

Temporary Cardiac Pacing Wire

K-Number: K173923 · 2018-08-02

ApplicantETHICON, Inc.
Decision Date2018-08-02
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Temporary Cardiac Pacing Wire is a medical device manufactured by ETHICON, Inc.. It received FDA 510(k) clearance on 2018-08-02 under approval number K173923. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Temporary Cardiac Pacing Wire?

Temporary Cardiac Pacing Wire is a medical device that received FDA 510(k) clearance on 2018-08-02. It is manufactured by ETHICON, Inc.. The 510(k) number is K173923.

When was Temporary Cardiac Pacing Wire approved by the FDA?

Temporary Cardiac Pacing Wire received FDA 510(k) clearance on 2018-08-02, under approval number K173923.

What company makes Temporary Cardiac Pacing Wire?

Temporary Cardiac Pacing Wire is manufactured by ETHICON, Inc..

What is the FDA product code for Temporary Cardiac Pacing Wire?

The FDA product code for Temporary Cardiac Pacing Wire is LDF.

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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.