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FDA 510(k)

PREGELLED DISPOSABLE ELECTRODE

K-Number: K781518 · 1978-10-06

Decision Date1978-10-06
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PREGELLED DISPOSABLE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Vente Medical Products, Inc.. It received FDA 510(k) clearance on 1978-10-06 under 510(k) number K781518. 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 PREGELLED DISPOSABLE ELECTRODE?

PREGELLED DISPOSABLE ELECTRODE is a medical device that received FDA 510(k) clearance on 1978-10-06. The listed applicant is Vente Medical Products, Inc.. The 510(k) number is K781518.

When did PREGELLED DISPOSABLE ELECTRODE receive FDA 510(k) clearance?

PREGELLED DISPOSABLE ELECTRODE received FDA 510(k) clearance on 1978-10-06, under 510(k) number K781518.

Who is the listed applicant for PREGELLED DISPOSABLE ELECTRODE?

The FDA 510(k) record lists Vente Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREGELLED DISPOSABLE ELECTRODE?

The FDA product code for PREGELLED DISPOSABLE ELECTRODE 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.

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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