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FDA 510(k)

NORTECH MODEL 86901000 ELECTRODE

K-Number: K903427 · 1990-08-17

ApplicantAndover Medical, Inc.
Decision Date1990-08-17
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NORTECH MODEL 86901000 ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Andover Medical, Inc.. It received FDA 510(k) clearance on 1990-08-17 under 510(k) number K903427. 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 NORTECH MODEL 86901000 ELECTRODE?

NORTECH MODEL 86901000 ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Andover Medical, Inc.. The 510(k) number is K903427.

When did NORTECH MODEL 86901000 ELECTRODE receive FDA 510(k) clearance?

NORTECH MODEL 86901000 ELECTRODE received FDA 510(k) clearance on 1990-08-17, under 510(k) number K903427.

Who is the listed applicant for NORTECH MODEL 86901000 ELECTRODE?

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

What is the FDA product code for NORTECH MODEL 86901000 ELECTRODE?

The FDA product code for NORTECH MODEL 86901000 ELECTRODE is GXY.

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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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