FDA 510(k)

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

Número K: K230336 · 2023-04-05

RequerenteLight Tree Ventures Europe B.V.

Data da decisão2023-04-05

Código do produtoOAP

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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