滑鞘細長
K 號：K173831 · 2018-05-08
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器材摘要
Glidesheath Slender is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corporation. It received FDA 510(k) clearance on 2018-05-08 under 510(k) number K173831. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Glidesheath Slender?
Glidesheath Slender is a medical device that received FDA 510(k) clearance on 2018-05-08. The listed applicant is Terumo Medical Corporation. The 510(k) number is K173831.
When did Glidesheath Slender receive FDA 510(k) clearance?
Glidesheath Slender received FDA 510(k) clearance on 2018-05-08, under 510(k) number K173831.
Who is the listed applicant for Glidesheath Slender?
The FDA 510(k) record lists Terumo Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Glidesheath Slender?
The FDA product code for Glidesheath Slender is DYB.
相關臨床試驗
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其他以 Terumo Medical Corporation 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：DYB）
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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