家用除毛設備，型號：精準觸控 Pro
K 號：K213830 · 2022-02-01
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器材摘要
常見問題
What is the Home use hair removal device, model: Precise Touch Pro?
Home use hair removal device, model: Precise Touch Pro is a medical device that received FDA 510(k) clearance on 2022-02-01. The listed applicant is Iluminage Beauty Co., Limited. The 510(k) number is K213830.
When did Home use hair removal device, model: Precise Touch Pro receive FDA 510(k) clearance?
Home use hair removal device, model: Precise Touch Pro received FDA 510(k) clearance on 2022-02-01, under 510(k) number K213830.
Who is the listed applicant for Home use hair removal device, model: Precise Touch Pro?
The FDA 510(k) record lists Iluminage Beauty Co., Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Home use hair removal device, model: Precise Touch Pro?
The FDA product code for Home use hair removal device, model: Precise Touch Pro is OHT.
相關臨床試驗
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。
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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