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FDA 510(k)

Evenflo Premium Double Electric Breast Pump (Model 4018)

N.º K: K230481 · 2023-11-03

SolicitanteEvenflo Feeding, Inc.
Fecha de decisión2023-11-03
Código de productoHGX
Comité asesorOB
DecisiónSubstantially Equivalent

Resumen del dispositivo

Evenflo Premium Double Electric Breast Pump (Model 4018) is the device name listed in this FDA 510(k) record. The listed applicant is Evenflo Feeding, Inc.. It received FDA 510(k) clearance on 2023-11-03 under 510(k) number K230481. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Evenflo Premium Double Electric Breast Pump (Model 4018)?

Evenflo Premium Double Electric Breast Pump (Model 4018) is a medical device that received FDA 510(k) clearance on 2023-11-03. The listed applicant is Evenflo Feeding, Inc.. The 510(k) number is K230481.

When did Evenflo Premium Double Electric Breast Pump (Model 4018) receive FDA 510(k) clearance?

Evenflo Premium Double Electric Breast Pump (Model 4018) received FDA 510(k) clearance on 2023-11-03, under 510(k) number K230481.

Who is the listed applicant for Evenflo Premium Double Electric Breast Pump (Model 4018)?

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

What is the FDA product code for Evenflo Premium Double Electric Breast Pump (Model 4018)?

The FDA product code for Evenflo Premium Double Electric Breast Pump (Model 4018) is HGX.

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Dispositivos relacionados (Código: HGX)

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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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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