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FDA 510(k)

DOCXS B SERIES ELECTRODES

K-Number: K020903 · 2002-09-26

ApplicantDocxs, LLC
Decision Date2002-09-26
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DOCXS B SERIES ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Docxs, LLC. It received FDA 510(k) clearance on 2002-09-26 under 510(k) number K020903. 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 DOCXS B SERIES ELECTRODES?

DOCXS B SERIES ELECTRODES is a medical device that received FDA 510(k) clearance on 2002-09-26. The listed applicant is Docxs, LLC. The 510(k) number is K020903.

When did DOCXS B SERIES ELECTRODES receive FDA 510(k) clearance?

DOCXS B SERIES ELECTRODES received FDA 510(k) clearance on 2002-09-26, under 510(k) number K020903.

Who is the listed applicant for DOCXS B SERIES ELECTRODES?

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

What is the FDA product code for DOCXS B SERIES ELECTRODES?

The FDA product code for DOCXS B SERIES ELECTRODES is GXY.

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: 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.

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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