FDA 510(k)

ライトベースの毛脱毛装置

K番号: K232846 · 2023-12-07

申請者Shenzhen Meik Beauty Industry Co., Ltd.

決定日2023-12-07

製品コードOHT

諮問委員会SU （以下のテキストは翻訳されていません。） Policy: medical-regulatory-v1

決定大幅同等

医療機器の概要

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.

よくある質問

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.

公式ソース

FDAデータベースで見る →

データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。

ライトベースの毛脱毛装置

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：OHT）

公式ソース