FDA 510(k)

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005

K-Number: K021537 · 2003-03-03

Decision Date2003-03-03

Product CodeGXY

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 is the device name listed in this FDA 510(k) record. The listed applicant is Vermont Medical, Inc.. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K021537. 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 MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005?

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Vermont Medical, Inc.. The 510(k) number is K021537.

When did MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 receive FDA 510(k) clearance?

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 received FDA 510(k) clearance on 2003-03-03, under 510(k) number K021537.

Who is the listed applicant for MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005?

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

What is the FDA product code for MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005?

The FDA product code for MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 is GXY.

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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.