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FDA 510(k)

AT

N.º K: K212645 · 2021-12-16

SolicitanteAt Glove Engineering Sdn. Bhd
Fecha de decisión2021-12-16
Código de productoLZA
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

AT is the device name listed in this FDA 510(k) record. The listed applicant is At Glove Engineering Sdn. Bhd. It received FDA 510(k) clearance on 2021-12-16 under 510(k) number K212645. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the AT?

AT is a medical device that received FDA 510(k) clearance on 2021-12-16. The listed applicant is At Glove Engineering Sdn. Bhd. The 510(k) number is K212645.

When did AT receive FDA 510(k) clearance?

AT received FDA 510(k) clearance on 2021-12-16, under 510(k) number K212645.

Who is the listed applicant for AT?

The FDA 510(k) record lists At Glove Engineering Sdn. Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AT?

The FDA product code for AT is LZA.

Literatura relacionada en PubMed

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Dispositivos relacionados (Código: LZA)

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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