FDA 510(k)

LUSTRE 3XPRESS 輕美療療貼片，型號：PR6001，PR5001

K 號：K230720 · 2023-07-03

決定日期2023-07-03

產品代碼OLP

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

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.

常見問題

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.

其他以 Light Tree Ventures Europe B.V. 為申請人之記錄

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相關器械（代碼：OLP）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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