FDA 510(k)

bili-hut

N.º K: K190899 · 2019-09-05

SolicitanteLittle Sparrows Technologies, Inc.

Fecha de decisión2019-09-05

Código de productoLBI

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

bili-hut is the device name listed in this FDA 510(k) record. The listed applicant is Little Sparrows Technologies, Inc.. It received FDA 510(k) clearance on 2019-09-05 under 510(k) number K190899. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the bili-hut?

bili-hut is a medical device that received FDA 510(k) clearance on 2019-09-05. The listed applicant is Little Sparrows Technologies, Inc.. The 510(k) number is K190899.

When did bili-hut receive FDA 510(k) clearance?

bili-hut received FDA 510(k) clearance on 2019-09-05, under 510(k) number K190899.

Who is the listed applicant for bili-hut?

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

What is the FDA product code for bili-hut?

The FDA product code for bili-hut is LBI.

Dispositivos relacionados (Código: LBI)

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.