HD聽診器
K 號：K201299 · 2020-07-10
廣告
器材摘要
HD Steth is the device name listed in this FDA 510(k) record. The listed applicant is Hd Medical, Inc.. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201299. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the HD Steth?
HD Steth is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Hd Medical, Inc.. The 510(k) number is K201299.
When did HD Steth receive FDA 510(k) clearance?
HD Steth received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201299.
Who is the listed applicant for HD Steth?
The FDA 510(k) record lists Hd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HD Steth?
The FDA product code for HD Steth is DQD.
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。
相關器械（代碼：DQD）
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。
廣告