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FDA 510(k)

美國製外科口罩

K 號:K210101 · 2022-01-26

決定日期2022-01-26
產品代碼FXX
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

American-Made Surgical Mask is the device name listed in this FDA 510(k) record. The listed applicant is Armbrust, Inc.. It received FDA 510(k) clearance on 2022-01-26 under 510(k) number K210101. 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 American-Made Surgical Mask?

American-Made Surgical Mask is a medical device that received FDA 510(k) clearance on 2022-01-26. The listed applicant is Armbrust, Inc.. The 510(k) number is K210101.

When did American-Made Surgical Mask receive FDA 510(k) clearance?

American-Made Surgical Mask received FDA 510(k) clearance on 2022-01-26, under 510(k) number K210101.

Who is the listed applicant for American-Made Surgical Mask?

The FDA 510(k) record lists Armbrust, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for American-Made Surgical Mask?

The FDA product code for American-Made Surgical Mask is FXX.

相關臨床試驗

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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。

官方來源

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