FDA 510(k)

Invu by Nuvo

N.º K: K221046 · 2022-05-06

Fecha de decisión2022-05-06

Código de productoLQK

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

Invu by Nuvo is the device name listed in this FDA 510(k) record. The listed applicant is Nuvo- Group , Ltd.. It received FDA 510(k) clearance on 2022-05-06 under 510(k) number K221046. The device is classified under product code LQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Invu by Nuvo?

Invu by Nuvo is a medical device that received FDA 510(k) clearance on 2022-05-06. The listed applicant is Nuvo- Group , Ltd.. The 510(k) number is K221046.

When did Invu by Nuvo receive FDA 510(k) clearance?

Invu by Nuvo received FDA 510(k) clearance on 2022-05-06, under 510(k) number K221046.

Who is the listed applicant for Invu by Nuvo?

The FDA 510(k) record lists Nuvo- Group , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Invu by Nuvo?

The FDA product code for Invu by Nuvo is LQK.

Otros registros que enlistan a Nuvo- Group , Ltd. 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.

K210025INVU by Nuvo K191401PregSense

Dispositivos relacionados (Código: LQK)

K253673M•care System (MW-20)Marani Health, Inc.K210025INVU by NuvoNuvo- Group , Ltd.K191401PregSenseNuvo- Group , Ltd.

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.