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FDA 510(k)

ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA

K-Number: K791003 · 1979-06-01

Decision Date1979-06-01
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1979-06-01 under 510(k) number K791003. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA?

ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA is a medical device that received FDA 510(k) clearance on 1979-06-01. The listed applicant is Physio-Control Corp.. The 510(k) number is K791003.

When did ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA receive FDA 510(k) clearance?

ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA received FDA 510(k) clearance on 1979-06-01, under 510(k) number K791003.

Who is the listed applicant for ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA?

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

What is the FDA product code for ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA?

The FDA product code for ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA is DRX.

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 Physio-Control 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.

View all 80 devices →

Related Devices (Code: DRX)

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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