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FDA 510(k)

LigaSure™ XP Maryland Jaw Sealer/Divider

K-Number: K223158 · 2023-01-23

ApplicantCovidien, LLC
Decision Date2023-01-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LigaSure™ XP Maryland Jaw Sealer/Divider is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, LLC. It received FDA 510(k) clearance on 2023-01-23 under 510(k) number K223158. 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 LigaSure™ XP Maryland Jaw Sealer/Divider?

LigaSure™ XP Maryland Jaw Sealer/Divider is a medical device that received FDA 510(k) clearance on 2023-01-23. The listed applicant is Covidien, LLC. The 510(k) number is K223158.

When did LigaSure™ XP Maryland Jaw Sealer/Divider receive FDA 510(k) clearance?

LigaSure™ XP Maryland Jaw Sealer/Divider received FDA 510(k) clearance on 2023-01-23, under 510(k) number K223158.

Who is the listed applicant for LigaSure™ XP Maryland Jaw Sealer/Divider?

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

What is the FDA product code for LigaSure™ XP Maryland Jaw Sealer/Divider?

The FDA product code for LigaSure™ XP Maryland Jaw Sealer/Divider is GEI.

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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.

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