FDA 510(k)

LYNX COBLATION Laryngeal Wand (72290254)

Número K: K253680 · 2026-03-25

Data da decisão2026-03-25

Código do produtoGEI

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

LYNX COBLATION Laryngeal Wand (72290254) is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-25 under 510(k) number K253680. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the LYNX COBLATION Laryngeal Wand (72290254)?

LYNX COBLATION Laryngeal Wand (72290254) is a medical device that received FDA 510(k) clearance on 2026-03-25. The listed applicant is ArthroCare Corporation. The 510(k) number is K253680.

When did LYNX COBLATION Laryngeal Wand (72290254) receive FDA 510(k) clearance?

LYNX COBLATION Laryngeal Wand (72290254) received FDA 510(k) clearance on 2026-03-25, under 510(k) number K253680.

Who is the listed applicant for LYNX COBLATION Laryngeal Wand (72290254)?

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

What is the FDA product code for LYNX COBLATION Laryngeal Wand (72290254)?

The FDA product code for LYNX COBLATION Laryngeal Wand (72290254) is GEI.

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