FDA 510(k)

3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask, Models 1804/1804S

K 號：K171116 · 2017-08-10

決定日期2017-08-10

產品代碼MSH

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

3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S is the device name listed in this FDA 510(k) record. The listed applicant is 3M Healthcare. It received FDA 510(k) clearance on 2017-08-10 under 510(k) number K171116. The device is classified under product code MSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S?

3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S is a medical device that received FDA 510(k) clearance on 2017-08-10. The listed applicant is 3M Healthcare. The 510(k) number is K171116.

When did 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S receive FDA 510(k) clearance?

3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S received FDA 510(k) clearance on 2017-08-10, under 510(k) number K171116.

Who is the listed applicant for 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S?

The FDA 510(k) record lists 3M Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S?

The FDA product code for 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S is MSH.

其他以 3M Healthcare 為申請人之記錄

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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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