植入式 fecal incontinence 裝置
PMA 核准號：P010020 · 2016-02-04
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器材摘要
Implanted fecal incontinence device is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2016-02-04. The device is classified under product code MIP. It was reviewed by the GU advisory panel.
常見問題
What is the Implanted fecal incontinence device?
Implanted fecal incontinence device is a medical device that received FDA 510(k) clearance on 2016-02-04. The listed applicant is Boston Scientific Corp.
When did Implanted fecal incontinence device receive FDA 510(k) clearance?
The clearance date for Implanted fecal incontinence device can be found in the official FDA records.
Who is the listed applicant for Implanted fecal incontinence device?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implanted fecal incontinence device?
The FDA product code for Implanted fecal incontinence device is MIP.
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。
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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