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FDA 510(k)

AMP por Method Mobility, AMP Plus (o +) por Method Mobility

N.º K: K231032 · 2023-05-10

SolicitanteMethod Mobility
Fecha de decisión2023-05-10
Código de productoITI
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

AMP by Method Mobility, AMP Plus (or +) by Method Mobility is the device name listed in this FDA 510(k) record. The listed applicant is Method Mobility. It received FDA 510(k) clearance on 2023-05-10 under 510(k) number K231032. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

AMP by Method Mobility, AMP Plus (or +) by Method Mobility is a medical device that received FDA 510(k) clearance on 2023-05-10. The listed applicant is Method Mobility. The 510(k) number is K231032.

When did AMP by Method Mobility, AMP Plus (or +) by Method Mobility receive FDA 510(k) clearance?

AMP by Method Mobility, AMP Plus (or +) by Method Mobility received FDA 510(k) clearance on 2023-05-10, under 510(k) number K231032.

Who is the listed applicant for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

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

What is the FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

The FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility is ITI.

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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