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FDA 510(k)

Leg and Foot Air Wave Pressure Therapy Device

N.º K: K223464 · 2023-03-14

SolicitanteZhangzhou Easepal Innovation CO , Ltd.
Fecha de decisión2023-03-14
Código de productoIRP
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

Leg and Foot Air Wave Pressure Therapy Device is the device name listed in this FDA 510(k) record. The listed applicant is Zhangzhou Easepal Innovation CO , Ltd.. It received FDA 510(k) clearance on 2023-03-14 under 510(k) number K223464. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Leg and Foot Air Wave Pressure Therapy Device?

Leg and Foot Air Wave Pressure Therapy Device is a medical device that received FDA 510(k) clearance on 2023-03-14. The listed applicant is Zhangzhou Easepal Innovation CO , Ltd.. The 510(k) number is K223464.

When did Leg and Foot Air Wave Pressure Therapy Device receive FDA 510(k) clearance?

Leg and Foot Air Wave Pressure Therapy Device received FDA 510(k) clearance on 2023-03-14, under 510(k) number K223464.

Who is the listed applicant for Leg and Foot Air Wave Pressure Therapy Device?

The FDA 510(k) record lists Zhangzhou Easepal Innovation CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Leg and Foot Air Wave Pressure Therapy Device?

The FDA product code for Leg and Foot Air Wave Pressure Therapy Device is IRP.

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