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FDA 510(k)

Seal Rite Non-Rebreathing Valve

N.º K: K152521 · 2016-06-03

SolicitanteThe Lifeguard Store, Inc.
Fecha de decisión2016-06-03
Código de productoCBP
Comité asesorAN
DecisiónSubstantially Equivalent

Resumen del dispositivo

Seal Rite Non-Rebreathing Valve is the device name listed in this FDA 510(k) record. The listed applicant is The Lifeguard Store, Inc.. It received FDA 510(k) clearance on 2016-06-03 under 510(k) number K152521. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Seal Rite Non-Rebreathing Valve?

Seal Rite Non-Rebreathing Valve is a medical device that received FDA 510(k) clearance on 2016-06-03. The listed applicant is The Lifeguard Store, Inc.. The 510(k) number is K152521.

When did Seal Rite Non-Rebreathing Valve receive FDA 510(k) clearance?

Seal Rite Non-Rebreathing Valve received FDA 510(k) clearance on 2016-06-03, under 510(k) number K152521.

Who is the listed applicant for Seal Rite Non-Rebreathing Valve?

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

What is the FDA product code for Seal Rite Non-Rebreathing Valve?

The FDA product code for Seal Rite Non-Rebreathing Valve is CBP.

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Dispositivos relacionados (Código: CBP)

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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