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FDA 510(k)

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

K-Number: K230720 · 2023-07-03

ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-07-03
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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