FDA 510(k)

FLOW FLEXTEND Wand (72290039)

N.º K: K254122 · 2026-03-30

Fecha de decisión2026-03-30

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

FLOW FLEXTEND Wand (72290039) is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-30 under 510(k) number K254122. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the FLOW FLEXTEND Wand (72290039)?

FLOW FLEXTEND Wand (72290039) is a medical device that received FDA 510(k) clearance on 2026-03-30. The listed applicant is ArthroCare Corporation. The 510(k) number is K254122.

When did FLOW FLEXTEND Wand (72290039) receive FDA 510(k) clearance?

FLOW FLEXTEND Wand (72290039) received FDA 510(k) clearance on 2026-03-30, under 510(k) number K254122.

Who is the listed applicant for FLOW FLEXTEND Wand (72290039)?

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 FLOW FLEXTEND Wand (72290039)?

The FDA product code for FLOW FLEXTEND Wand (72290039) is GEI.

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Fuente oficial

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