FDA 510(k)

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001

Numéro K : K230720 · 2023-07-03

DemandeurLight Tree Ventures Europe B.V.

Date de décision2023-07-03

Code produitOLP

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 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 2023-07-03 under 510(k) number K230720. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is a medical device that received FDA 510(k) clearance on 2023-07-03. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K230720.

When did LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 receive FDA 510(k) clearance?

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 received FDA 510(k) clearance on 2023-07-03, under 510(k) number K230720.

Who is the listed applicant for LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

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 LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

The FDA product code for LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is OLP.

Essais cliniques associés

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Source officielle

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