FDA 510(k)

THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG

K-Number: K020445 · 2002-05-10

Decision Date2002-05-10

Product CodeGXY

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG is the device name listed in this FDA 510(k) record. The listed applicant is The Electrode Store, Inc.. It received FDA 510(k) clearance on 2002-05-10 under 510(k) number K020445. 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 THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG?

THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG is a medical device that received FDA 510(k) clearance on 2002-05-10. The listed applicant is The Electrode Store, Inc.. The 510(k) number is K020445.

When did THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG receive FDA 510(k) clearance?

THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG received FDA 510(k) clearance on 2002-05-10, under 510(k) number K020445.

Who is the listed applicant for THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG?

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

What is the FDA product code for THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG?

The FDA product code for THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMG is GXY.

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Other records listing The Electrode Store, Inc. as applicant

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Related Devices (Code: GXY)

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Official Source

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