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FDA 510(k)

光基脫毛設備

K 號：K232846 · 2023-12-07

申請人Shenzhen Meik Beauty Industry Co., Ltd.
決定日期2023-12-07
產品代碼OHT
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

Light Based Hair Removal Device is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Meik Beauty Industry Co., Ltd.. It received FDA 510(k) clearance on 2023-12-07 under 510(k) number K232846. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Light Based Hair Removal Device?

Light Based Hair Removal Device is a medical device that received FDA 510(k) clearance on 2023-12-07. The listed applicant is Shenzhen Meik Beauty Industry Co., Ltd.. The 510(k) number is K232846.

When did Light Based Hair Removal Device receive FDA 510(k) clearance?

Light Based Hair Removal Device received FDA 510(k) clearance on 2023-12-07, under 510(k) number K232846.

Who is the listed applicant for Light Based Hair Removal Device?

The FDA 510(k) record lists Shenzhen Meik Beauty Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Light Based Hair Removal Device?

The FDA product code for Light Based Hair Removal Device is OHT.

相關臨床試驗

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相關器械（代碼：OHT）

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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