FDA 510(k)

LED 唇部修護器，型號：ZC-05

K 號：K223642 · 2023-03-09

決定日期2023-03-09

產品代碼ILY

諮詢委員會PM

決定相當於

器材摘要

LED Lip Perfector, model: ZC-05 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 2023-03-09 under 510(k) number K223642. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LED Lip Perfector, model: ZC-05?

LED Lip Perfector, model: ZC-05 is a medical device that received FDA 510(k) clearance on 2023-03-09. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K223642.

When did LED Lip Perfector, model: ZC-05 receive FDA 510(k) clearance?

LED Lip Perfector, model: ZC-05 received FDA 510(k) clearance on 2023-03-09, under 510(k) number K223642.

Who is the listed applicant for LED Lip Perfector, model: ZC-05?

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 LED Lip Perfector, model: ZC-05?

The FDA product code for LED Lip Perfector, model: ZC-05 is ILY.

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：ILY）

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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