ECG ELECTRODES, PEDIATRIC-MICROPOROUS TA
K-Number: K791003 · 1979-06-01
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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