FDA 510(k)

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)

N.º K: K230336 · 2023-04-05

SolicitanteLight Tree Ventures Europe B.V.

Fecha de decisión2023-04-05

Código de productoOAP

Comité asesorPM

DecisiónSubstantially Equivalent

Resumen del dispositivo

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is the device name listed in this FDA 510(k) record. The listed applicant is Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-04-05 under 510(k) number K230336. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K230336.

When did CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) receive FDA 510(k) clearance?

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) received FDA 510(k) clearance on 2023-04-05, under 510(k) number K230336.

Who is the listed applicant for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

The FDA 510(k) record lists Light Tree Ventures Europe B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

The FDA product code for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is OAP.

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Otros registros que enlistan a Light Tree Ventures Europe B.V. como solicitante

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Dispositivos relacionados (Código: OAP)

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Fuente oficial

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