FDA 510(k)

FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS

K-Number: K070162 · 2007-03-06

ApplicantValleylab,A Division of Tyco Healthcare Group LP

Decision Date2007-03-06

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab,A Division of Tyco Healthcare Group LP. It received FDA 510(k) clearance on 2007-03-06 under 510(k) number K070162. 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; LIGASURE INSTRUMENTS?

FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2007-03-06. The listed applicant is Valleylab,A Division of Tyco Healthcare Group LP. The 510(k) number is K070162.

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

FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS received FDA 510(k) clearance on 2007-03-06, under 510(k) number K070162.

Who is the listed applicant for FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS?

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

What is the FDA product code for FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS?

The FDA product code for FORCETRIAD ELECTROSURGICAL GENERATOR; LIGASURE INSTRUMENTS is GEI.

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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.