Oral-B iO 測試駕駛功率牙刷試用方案組
K 號：K200881 · 2020-08-27
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器材摘要
Oral-B iO Test Drive Power Brush Trial Program Kit is the device name listed in this FDA 510(k) record. The listed applicant is The Procter & Gamble Company. It received FDA 510(k) clearance on 2020-08-27 under 510(k) number K200881. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Oral-B iO Test Drive Power Brush Trial Program Kit?
Oral-B iO Test Drive Power Brush Trial Program Kit is a medical device that received FDA 510(k) clearance on 2020-08-27. The listed applicant is The Procter & Gamble Company. The 510(k) number is K200881.
When did Oral-B iO Test Drive Power Brush Trial Program Kit receive FDA 510(k) clearance?
Oral-B iO Test Drive Power Brush Trial Program Kit received FDA 510(k) clearance on 2020-08-27, under 510(k) number K200881.
Who is the listed applicant for Oral-B iO Test Drive Power Brush Trial Program Kit?
The FDA 510(k) record lists The Procter & Gamble Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oral-B iO Test Drive Power Brush Trial Program Kit?
The FDA product code for Oral-B iO Test Drive Power Brush Trial Program Kit is JEQ.
相關臨床試驗
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其他以 The Procter & Gamble Company 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。
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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