FDA 510(k)

PMW01 調節口罩等級 1

K 號：K211772 · 2021-12-06

決定日期2021-12-06

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

PMW01 Procedure Mask Level 1 is the device name listed in this FDA 510(k) record. The listed applicant is Defender Safety, Inc.. It received FDA 510(k) clearance on 2021-12-06 under 510(k) number K211772. 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 PMW01 Procedure Mask Level 1?

PMW01 Procedure Mask Level 1 is a medical device that received FDA 510(k) clearance on 2021-12-06. The listed applicant is Defender Safety, Inc.. The 510(k) number is K211772.

When did PMW01 Procedure Mask Level 1 receive FDA 510(k) clearance?

PMW01 Procedure Mask Level 1 received FDA 510(k) clearance on 2021-12-06, under 510(k) number K211772.

Who is the listed applicant for PMW01 Procedure Mask Level 1?

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

What is the FDA product code for PMW01 Procedure Mask Level 1?

The FDA product code for PMW01 Procedure Mask Level 1 is FXX.

其他以 Defender Safety, Inc. 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。

K210705防護安全程序口罩第1級，防護安全程序口罩第3級，防護安全外科口罩第3級

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

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