FDA 510(k)

KOWA FM-600

N.º K: K261255 · 2026-09-11

SolicitanteKowa Company, Ltd. Chofu Factory

Fecha de decisión2026-09-11

Código de productoMYC

Comité asesorOP

DecisiónSubstantially Equivalent

Resumen del dispositivo

KOWA FM-600 is the device name listed in this FDA 510(k) record. The listed applicant is Kowa Company, Ltd. Chofu Factory. It received FDA 510(k) clearance on 2026-09-11 under 510(k) number K261255. The device is classified under product code MYC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the KOWA FM-600?

KOWA FM-600 is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Kowa Company, Ltd. Chofu Factory. The 510(k) number is K261255.

When did KOWA FM-600 receive FDA 510(k) clearance?

KOWA FM-600 received FDA 510(k) clearance on 2026-09-11, under 510(k) number K261255.

Who is the listed applicant for KOWA FM-600?

The FDA 510(k) record lists Kowa Company, Ltd. Chofu Factory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOWA FM-600?

The FDA product code for KOWA FM-600 is MYC.

Dispositivos relacionados (Código: MYC)

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Fuente oficial

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