熱塑性口罩
K 號：K192102 · 2019-09-25
廣告
器材摘要
Thermoplastic Masks is the device name listed in this FDA 510(k) record. The listed applicant is Aktina Medical Corporation. It received FDA 510(k) clearance on 2019-09-25 under 510(k) number K192102. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Thermoplastic Masks?
Thermoplastic Masks is a medical device that received FDA 510(k) clearance on 2019-09-25. The listed applicant is Aktina Medical Corporation. The 510(k) number is K192102.
When did Thermoplastic Masks receive FDA 510(k) clearance?
Thermoplastic Masks received FDA 510(k) clearance on 2019-09-25, under 510(k) number K192102.
Who is the listed applicant for Thermoplastic Masks?
The FDA 510(k) record lists Aktina Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Thermoplastic Masks?
The FDA product code for Thermoplastic Masks is IYE.
相關臨床試驗
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其他以 Aktina 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：IYE）
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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