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FDA 510(k)

Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile

N.º K: K221014 · 2022-10-17

SolicitanteEffortless Oxygen, LLC
Fecha de decisión2022-10-17
Código de productoNFB
Comité asesorAN
DecisiónSubstantially Equivalent

Resumen del dispositivo

Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile is the device name listed in this FDA 510(k) record. The listed applicant is Effortless Oxygen, LLC. It received FDA 510(k) clearance on 2022-10-17 under 510(k) number K221014. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile?

Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile is a medical device that received FDA 510(k) clearance on 2022-10-17. The listed applicant is Effortless Oxygen, LLC. The 510(k) number is K221014.

When did Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile receive FDA 510(k) clearance?

Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile received FDA 510(k) clearance on 2022-10-17, under 510(k) number K221014.

Who is the listed applicant for Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile?

The FDA 510(k) record lists Effortless Oxygen, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile?

The FDA product code for Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile is NFB.

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Dispositivos relacionados (Código: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter Labs

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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