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FDA 510(k)

MedHealth DVT compression Devices MHH900S/MHH900E

N.º K: K231801 · 2023-12-14

SolicitanteMedhealth Medical Limited
Fecha de decisión2023-12-14
Código de productoJOW
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

MedHealth DVT compression Devices MHH900S/MHH900E is the device name listed in this FDA 510(k) record. The listed applicant is Medhealth Medical Limited. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K231801. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MedHealth DVT compression Devices MHH900S/MHH900E?

MedHealth DVT compression Devices MHH900S/MHH900E is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Medhealth Medical Limited. The 510(k) number is K231801.

When did MedHealth DVT compression Devices MHH900S/MHH900E receive FDA 510(k) clearance?

MedHealth DVT compression Devices MHH900S/MHH900E received FDA 510(k) clearance on 2023-12-14, under 510(k) number K231801.

Who is the listed applicant for MedHealth DVT compression Devices MHH900S/MHH900E?

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

What is the FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E?

The FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E is JOW.

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Dispositivos relacionados (Código: JOW)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

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