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FDA 510(k)

CARDIAC PACING ELECTRODES

K-Number: K812517 · 1981-10-13

Decision Date1981-10-13
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIAC PACING ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Medics Instrument Corp.. It received FDA 510(k) clearance on 1981-10-13 under 510(k) number K812517. 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 CARDIAC PACING ELECTRODES?

CARDIAC PACING ELECTRODES is a medical device that received FDA 510(k) clearance on 1981-10-13. The listed applicant is Medics Instrument Corp.. The 510(k) number is K812517.

When did CARDIAC PACING ELECTRODES receive FDA 510(k) clearance?

CARDIAC PACING ELECTRODES received FDA 510(k) clearance on 1981-10-13, under 510(k) number K812517.

Who is the listed applicant for CARDIAC PACING ELECTRODES?

The FDA 510(k) record lists Medics Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIAC PACING ELECTRODES?

The FDA product code for CARDIAC PACING ELECTRODES 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 Medics Instrument Corp. 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

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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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