Amsel 遮斷器設備
K 號：K172479 · 2017-09-14
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器材摘要
Amsel Occluder Device is the device name listed in this FDA 510(k) record. The listed applicant is Amsel Medical. It received FDA 510(k) clearance on 2017-09-14 under 510(k) number K172479. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Amsel Occluder Device?
Amsel Occluder Device is a medical device that received FDA 510(k) clearance on 2017-09-14. The listed applicant is Amsel Medical. The 510(k) number is K172479.
When did Amsel Occluder Device receive FDA 510(k) clearance?
Amsel Occluder Device received FDA 510(k) clearance on 2017-09-14, under 510(k) number K172479.
Who is the listed applicant for Amsel Occluder Device?
The FDA 510(k) record lists Amsel Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Amsel Occluder Device?
The FDA product code for Amsel Occluder Device is FZP.
相關臨床試驗
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相關器械（代碼：FZP）
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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