FDA 510(k)

MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE

K-Number: K905446 · 1991-02-05

ApplicantMedtronic Andover Medical, Inc.

Decision Date1991-02-05

Product CodeDRX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDITRONIC ANDOVER MEDICAL MODEL 1690 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 1991-02-05 under 510(k) number K905446. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE?

MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE is a medical device that received FDA 510(k) clearance on 1991-02-05. The listed applicant is Medtronic Andover Medical, Inc.. The 510(k) number is K905446.

When did MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE receive FDA 510(k) clearance?

MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE received FDA 510(k) clearance on 1991-02-05, under 510(k) number K905446.

Who is the listed applicant for MEDITRONIC ANDOVER MEDICAL MODEL 1690 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 MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE?

The FDA product code for MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODE is DRX.

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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.