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FDA 510(k)

FORCETRIAD ELECTROSURGICAL GENERATOR

K-Number: K110268 · 2011-05-31

ApplicantCovidien Lp, Formerly Know AS Valleylab, A Divison
Decision Date2011-05-31
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCETRIAD ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Covidien Lp, Formerly Know AS Valleylab, A Divison. It received FDA 510(k) clearance on 2011-05-31 under 510(k) number K110268. 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 ELECTROSURGICAL GENERATOR?

FORCETRIAD ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2011-05-31. The listed applicant is Covidien Lp, Formerly Know AS Valleylab, A Divison. The 510(k) number is K110268.

When did FORCETRIAD ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

FORCETRIAD ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2011-05-31, under 510(k) number K110268.

Who is the listed applicant for FORCETRIAD ELECTROSURGICAL GENERATOR?

The FDA 510(k) record lists Covidien Lp, Formerly Know AS Valleylab, A Divison as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCETRIAD ELECTROSURGICAL GENERATOR?

The FDA product code for FORCETRIAD ELECTROSURGICAL GENERATOR is GEI.

Related Clinical Trials

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Other records listing Covidien Lp, Formerly Know AS Valleylab, A Divison 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.

K072687VALLEYLAB MICROWAVE ABLATION GENERATOR

Related Devices (Code: GEI)

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.

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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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