外科口罩
K 號：K203161 · 2022-01-20
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器材摘要
Surgical Face Mask is the device name listed in this FDA 510(k) record. The listed applicant is Wuhan Raytex Protection Co., Ltd.. It received FDA 510(k) clearance on 2022-01-20 under 510(k) number K203161. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Surgical Face Mask?
Surgical Face Mask is a medical device that received FDA 510(k) clearance on 2022-01-20. The listed applicant is Wuhan Raytex Protection Co., Ltd.. The 510(k) number is K203161.
When did Surgical Face Mask receive FDA 510(k) clearance?
Surgical Face Mask received FDA 510(k) clearance on 2022-01-20, under 510(k) number K203161.
Who is the listed applicant for Surgical Face Mask?
The FDA 510(k) record lists Wuhan Raytex Protection Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Surgical Face Mask?
The FDA product code for Surgical Face Mask is FXX.
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相關器械（代碼：FXX）
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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