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FDA 510(k)

Lumilisse IPL Hair Remover

N.º K: K172791 · 2018-01-18

SolicitanteConair Corporation
Fecha de decisión2018-01-18
Código de productoOHT
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Lumilisse IPL Hair Remover is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corporation. It received FDA 510(k) clearance on 2018-01-18 under 510(k) number K172791. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Lumilisse IPL Hair Remover?

Lumilisse IPL Hair Remover is a medical device that received FDA 510(k) clearance on 2018-01-18. The listed applicant is Conair Corporation. The 510(k) number is K172791.

When did Lumilisse IPL Hair Remover receive FDA 510(k) clearance?

Lumilisse IPL Hair Remover received FDA 510(k) clearance on 2018-01-18, under 510(k) number K172791.

Who is the listed applicant for Lumilisse IPL Hair Remover?

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

What is the FDA product code for Lumilisse IPL Hair Remover?

The FDA product code for Lumilisse IPL Hair Remover is OHT.

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Dispositivos relacionados (Código: OHT)

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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