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FDA 510(k)

DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K

K-Number: K952176 · 1995-09-25

ApplicantMedicotest, Inc.
Decision Date1995-09-25
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K is the device name listed in this FDA 510(k) record. The listed applicant is Medicotest, Inc.. It received FDA 510(k) clearance on 1995-09-25 under 510(k) number K952176. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K?

DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K is a medical device that received FDA 510(k) clearance on 1995-09-25. The listed applicant is Medicotest, Inc.. The 510(k) number is K952176.

When did DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K receive FDA 510(k) clearance?

DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K received FDA 510(k) clearance on 1995-09-25, under 510(k) number K952176.

Who is the listed applicant for DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K?

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 DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K?

The FDA product code for DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K is GXY.

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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 ELECTRODESK941568K-10-VS, DA-05-VS, RECORDING ELECTRODESK931426NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODEK931430CUTANEOUS ELECTRODE

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Related Devices (Code: GXY)

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.

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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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