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FDA 510(k)

MEDICOTEST ELECTRODE PASTE

K-Number: K821539 · 1982-07-02

ApplicantMedicotest, Inc.
Decision Date1982-07-02
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDICOTEST ELECTRODE PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Medicotest, Inc.. It received FDA 510(k) clearance on 1982-07-02 under 510(k) number K821539. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICOTEST ELECTRODE PASTE?

MEDICOTEST ELECTRODE PASTE is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Medicotest, Inc.. The 510(k) number is K821539.

When did MEDICOTEST ELECTRODE PASTE receive FDA 510(k) clearance?

MEDICOTEST ELECTRODE PASTE received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821539.

Who is the listed applicant for MEDICOTEST ELECTRODE PASTE?

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

What is the FDA product code for MEDICOTEST ELECTRODE PASTE?

The FDA product code for MEDICOTEST ELECTRODE PASTE is GYB.

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Other records listing Medicotest, 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.

K983597NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODESK970639NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-KK961643MEDICOTEST ECG ELECTRODESK952176DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-KK941568K-10-VS, DA-05-VS, RECORDING ELECTRODESK931430CUTANEOUS ELECTRODE

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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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