醫用設備名稱：Yglo瘡瘡去除器
K 號：K210529 · 2021-05-06
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器材摘要
Dr. Yglo Wart Remover is the device name listed in this FDA 510(k) record. The listed applicant is Theotclab Healthcare B.V.. It received FDA 510(k) clearance on 2021-05-06 under 510(k) number K210529. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Dr. Yglo Wart Remover?
Dr. Yglo Wart Remover is a medical device that received FDA 510(k) clearance on 2021-05-06. The listed applicant is Theotclab Healthcare B.V.. The 510(k) number is K210529.
When did Dr. Yglo Wart Remover receive FDA 510(k) clearance?
Dr. Yglo Wart Remover received FDA 510(k) clearance on 2021-05-06, under 510(k) number K210529.
Who is the listed applicant for Dr. Yglo Wart Remover?
The FDA 510(k) record lists Theotclab Healthcare B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dr. Yglo Wart Remover?
The FDA product code for Dr. Yglo Wart Remover is GEH.
相關臨床試驗
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其他以 Theotclab Healthcare B.V. 為申請人之記錄
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：GEH）
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
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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