FDA 510(k)

LYNX COBLATION 코르넬 워드 (72290254)

K-번호: K253680 · 2026-03-25

결정일2026-03-25

제품 코드GEI

자문 위원회SU

결정Substantially Equivalent

기기 요약

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.

자주 묻는 질문

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.

ArthroCare Corporation를 신청인으로 등재한 기타 기록

K254122플로우 플렉스텐 와드 (72290039)K240964플로우 90 워ند K232290인텔리오 셔프트 시스템 K230914ARIS¿ COBLATION¿ 터빈 감소 와이드 (72290113); WEREWOLF COBLATION 시스템 (72290144); WEREWOLF+ COBLATION 시스템 (72290146)K220563Ambient HipVac 50 Wand with Integrated Finger Switches, RF20000 COBLATION System, WEREWOLF COBLATION System, WEREWOLF+ COBLATION System K210423Werewolf+ Coblation System, Werewolf+ Controller, Werewolf Fastseal 6.0 Hemostasis Wand

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