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FDA 510(k)

FORCETRIAD

K-Number: K102913 · 2011-05-06

ApplicantCovidien, Formerly Valleylab, A Division of Tyco H
Decision Date2011-05-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCETRIAD is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, Formerly Valleylab, A Division of Tyco H. It received FDA 510(k) clearance on 2011-05-06 under 510(k) number K102913. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCETRIAD?

FORCETRIAD is a medical device that received FDA 510(k) clearance on 2011-05-06. The listed applicant is Covidien, Formerly Valleylab, A Division of Tyco H. The 510(k) number is K102913.

When did FORCETRIAD receive FDA 510(k) clearance?

FORCETRIAD received FDA 510(k) clearance on 2011-05-06, under 510(k) number K102913.

Who is the listed applicant for FORCETRIAD?

The FDA 510(k) record lists Covidien, Formerly Valleylab, A Division of Tyco H as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCETRIAD?

The FDA product code for FORCETRIAD is GEI.

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Other records listing Covidien, Formerly Valleylab, A Division of Tyco H as applicant

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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.

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