FDA 510(k)

V-PVP

N.º K: K232125 · 2024-03-20

Fecha de decisión2024-03-20

Código de productoMQL

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

V-PVP is the device name listed in this FDA 510(k) record. The listed applicant is Vitromed GmbH. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K232125. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the V-PVP?

V-PVP is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Vitromed GmbH. The 510(k) number is K232125.

When did V-PVP receive FDA 510(k) clearance?

V-PVP received FDA 510(k) clearance on 2024-03-20, under 510(k) number K232125.

Who is the listed applicant for V-PVP?

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

What is the FDA product code for V-PVP?

The FDA product code for V-PVP is MQL.

Otros registros que enlistan a Vitromed GmbH como solicitante

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.

K241833V-GRAD K240176V-VITFREEZE and V-VITWARM K222606V-HYADASE K223117V-SPERM WASH K193285V-ONESTEP K192146V-DENUPET

Ver todos los 7 dispositivos →

Dispositivos relacionados (Código: MQL)

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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.