FDA 510(k)

LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated

Numéro K : K261070 · 2026-09-15

Date de décision2026-09-15

Code produitGEI

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, LLC. It received FDA 510(k) clearance on 2026-09-15 under 510(k) number K261070. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?

LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated is a medical device that received FDA 510(k) clearance on 2026-09-15. The listed applicant is Covidien, LLC. The 510(k) number is K261070.

When did LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated receive FDA 510(k) clearance?

LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated received FDA 510(k) clearance on 2026-09-15, under 510(k) number K261070.

Who is the listed applicant for LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?

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™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?

The FDA product code for LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated is GEI.

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Source officielle

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