FDA 510(k)

The POD

N.º K: K182820 · 2019-07-17

Fecha de decisión2019-07-17

Código de productoMQC

DecisiónSubstantially Equivalent

Resumen del dispositivo

The POD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Facialdontics, LLC. It received FDA 510(k) clearance on 2019-07-17 under 510(k) number K182820. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the The POD?

The POD is a medical device that received FDA 510(k) clearance on 2019-07-17. The listed applicant is Advanced Facialdontics, LLC. The 510(k) number is K182820.

When did The POD receive FDA 510(k) clearance?

The POD received FDA 510(k) clearance on 2019-07-17, under 510(k) number K182820.

Who is the listed applicant for The POD?

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

What is the FDA product code for The POD?

The FDA product code for The POD is MQC.

Otros registros que enlistan a Advanced Facialdontics, LLC 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.

K192581The NightBlocks Appliance

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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.