良好根 ST
K 號：K170950 · 2017-12-20
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器材摘要
Well-Root ST is the device name listed in this FDA 510(k) record. The listed applicant is Vericom Co., Ltd.. It received FDA 510(k) clearance on 2017-12-20 under 510(k) number K170950. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Well-Root ST?
Well-Root ST is a medical device that received FDA 510(k) clearance on 2017-12-20. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K170950.
When did Well-Root ST receive FDA 510(k) clearance?
Well-Root ST received FDA 510(k) clearance on 2017-12-20, under 510(k) number K170950.
Who is the listed applicant for Well-Root ST?
The FDA 510(k) record lists Vericom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Well-Root ST?
The FDA product code for Well-Root ST is KIF.
其他以 Vericom Co., Ltd. 為申請人之記錄
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相關器械（代碼：KIF）
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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