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FDA 510(k)

NORTECH MODEL 87202204 ELECTRODE

K-Number: K903554 · 1990-08-30

ApplicantMedtronic Andover Medical, Inc.
Decision Date1990-08-30
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NORTECH MODEL 87202204 ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Andover Medical, Inc.. It received FDA 510(k) clearance on 1990-08-30 under 510(k) number K903554. 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 87202204 ELECTRODE?

NORTECH MODEL 87202204 ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-08-30. The listed applicant is Medtronic Andover Medical, Inc.. The 510(k) number is K903554.

When did NORTECH MODEL 87202204 ELECTRODE receive FDA 510(k) clearance?

NORTECH MODEL 87202204 ELECTRODE received FDA 510(k) clearance on 1990-08-30, under 510(k) number K903554.

Who is the listed applicant for NORTECH MODEL 87202204 ELECTRODE?

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

What is the FDA product code for NORTECH MODEL 87202204 ELECTRODE?

The FDA product code for NORTECH MODEL 87202204 ELECTRODE is GXY.

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Other records listing Medtronic Andover Medical, 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.

K910494RESTING EKG ELECTRODE SERIESK905446MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODEK903018MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002K882174MODIFIED MODEL 5455 DISPOSABLE SURGICAL CABLEK852469SAF-D-FIB

Related Devices (Code: GXY)

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Official Source

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