凤凰傷口維織物
K 號：K173544 · 2018-03-02
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器材摘要
Phoenix Wound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Nanofiber Solutions, Inc.. It received FDA 510(k) clearance on 2018-03-02 under 510(k) number K173544. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.
常見問題
What is the Phoenix Wound Matrix?
Phoenix Wound Matrix is a medical device that received FDA 510(k) clearance on 2018-03-02. The listed applicant is Nanofiber Solutions, Inc.. The 510(k) number is K173544.
When did Phoenix Wound Matrix receive FDA 510(k) clearance?
Phoenix Wound Matrix received FDA 510(k) clearance on 2018-03-02, under 510(k) number K173544.
Who is the listed applicant for Phoenix Wound Matrix?
The FDA 510(k) record lists Nanofiber Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Phoenix Wound Matrix?
The FDA product code for Phoenix Wound Matrix is QSZ.
相關臨床試驗
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相關器械（代碼：QSZ）
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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