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FDA 510(k)

Kinsa QuickCare Thermometer

N.º K: K173730 · 2018-01-17

SolicitanteKinsa, Inc.
Fecha de decisión2018-01-17
Código de productoFLL
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

Kinsa QuickCare Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Kinsa, Inc.. It received FDA 510(k) clearance on 2018-01-17 under 510(k) number K173730. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Kinsa QuickCare Thermometer?

Kinsa QuickCare Thermometer is a medical device that received FDA 510(k) clearance on 2018-01-17. The listed applicant is Kinsa, Inc.. The 510(k) number is K173730.

When did Kinsa QuickCare Thermometer receive FDA 510(k) clearance?

Kinsa QuickCare Thermometer received FDA 510(k) clearance on 2018-01-17, under 510(k) number K173730.

Who is the listed applicant for Kinsa QuickCare Thermometer?

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

What is the FDA product code for Kinsa QuickCare Thermometer?

The FDA product code for Kinsa QuickCare Thermometer is FLL.

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Dispositivos relacionados (Código: FLL)

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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