Temporary Cardiac Pacing Wire
K-Number: K173923 · 2018-08-02
Device Summary
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. The listed applicant is ETHICON, Inc.. The 510(k) number is K173923.
When did Temporary Cardiac Pacing Wire receive FDA 510(k) clearance?
Temporary Cardiac Pacing Wire received FDA 510(k) clearance on 2018-08-02, under 510(k) number K173923.
Who is the listed applicant for Temporary Cardiac Pacing Wire?
The FDA 510(k) record lists ETHICON, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Temporary Cardiac Pacing Wire?
The FDA product code for Temporary Cardiac Pacing Wire is LDF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing ETHICON, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LDF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.