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FDA 510(k)

LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER

K-Number: K102470 · 2011-02-07

ApplicantCovidien, Formerly Valleylab,
Decision Date2011-02-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, Formerly Valleylab,. It received FDA 510(k) clearance on 2011-02-07 under 510(k) number K102470. 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 LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER?

LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER is a medical device that received FDA 510(k) clearance on 2011-02-07. The listed applicant is Covidien, Formerly Valleylab,. The 510(k) number is K102470.

When did LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER receive FDA 510(k) clearance?

LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER received FDA 510(k) clearance on 2011-02-07, under 510(k) number K102470.

Who is the listed applicant for LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER?

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

What is the FDA product code for LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER?

The FDA product code for LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER 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.

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