FDA 510(k)

GYRUS ACMI PK BUTTON ELECTRODE

K-Number: K093181 · 2010-02-24

Decision Date2010-02-24

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

GYRUS ACMI PK BUTTON ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Acmi, Inc.. It received FDA 510(k) clearance on 2010-02-24 under 510(k) number K093181. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYRUS ACMI PK BUTTON ELECTRODE?

GYRUS ACMI PK BUTTON ELECTRODE is a medical device that received FDA 510(k) clearance on 2010-02-24. The listed applicant is Gyrus Acmi, Inc.. The 510(k) number is K093181.

When did GYRUS ACMI PK BUTTON ELECTRODE receive FDA 510(k) clearance?

GYRUS ACMI PK BUTTON ELECTRODE received FDA 510(k) clearance on 2010-02-24, under 510(k) number K093181.

Who is the listed applicant for GYRUS ACMI PK BUTTON ELECTRODE?

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

What is the FDA product code for GYRUS ACMI PK BUTTON ELECTRODE?

The FDA product code for GYRUS ACMI PK BUTTON ELECTRODE is FAS.

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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.