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FDA 510(k)

Negative Pressure Wound Therapy Device (V-Move, V-Grand)

N.º K: K241023 · 2024-08-19

SolicitanteMed Way, Inc.
Fecha de decisión2024-08-19
Código de productoOMP
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Negative Pressure Wound Therapy Device (V-Move, V-Grand) is the device name listed in this FDA 510(k) record. The listed applicant is Med Way, Inc.. It received FDA 510(k) clearance on 2024-08-19 under 510(k) number K241023. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

Negative Pressure Wound Therapy Device (V-Move, V-Grand) is a medical device that received FDA 510(k) clearance on 2024-08-19. The listed applicant is Med Way, Inc.. The 510(k) number is K241023.

When did Negative Pressure Wound Therapy Device (V-Move, V-Grand) receive FDA 510(k) clearance?

Negative Pressure Wound Therapy Device (V-Move, V-Grand) received FDA 510(k) clearance on 2024-08-19, under 510(k) number K241023.

Who is the listed applicant for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

The FDA 510(k) record lists Med Way, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

The FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand) is OMP.

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Dispositivos relacionados (Código: OMP)

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

Ver en la base de datos de la FDA →

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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