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FDA 510(k)

ETHICON* TEMP. CARDIAC PACING WIRE

K-Number: K813138 · 1981-12-10

ApplicantETHICON, Inc.
Decision Date1981-12-10
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ETHICON* TEMP. CARDIAC PACING WIRE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1981-12-10 under 510(k) number K813138. 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 ETHICON* TEMP. CARDIAC PACING WIRE?

ETHICON* TEMP. CARDIAC PACING WIRE is a medical device that received FDA 510(k) clearance on 1981-12-10. The listed applicant is ETHICON, Inc.. The 510(k) number is K813138.

When did ETHICON* TEMP. CARDIAC PACING WIRE receive FDA 510(k) clearance?

ETHICON* TEMP. CARDIAC PACING WIRE received FDA 510(k) clearance on 1981-12-10, under 510(k) number K813138.

Who is the listed applicant for ETHICON* TEMP. 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 ETHICON* TEMP. CARDIAC PACING WIRE?

The FDA product code for ETHICON* TEMP. 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.

View all 195 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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