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FDA 510(k)

灣櫻美國外科口罩第3級

K 號:K211097 · 2021-09-22

決定日期2021-09-22
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

Banyan USA Surgical Mask Level 3 is the device name listed in this FDA 510(k) record. The listed applicant is Banyan USA, LLC. It received FDA 510(k) clearance on 2021-09-22 under 510(k) number K211097. 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 Banyan USA Surgical Mask Level 3?

Banyan USA Surgical Mask Level 3 is a medical device that received FDA 510(k) clearance on 2021-09-22. The listed applicant is Banyan USA, LLC. The 510(k) number is K211097.

When did Banyan USA Surgical Mask Level 3 receive FDA 510(k) clearance?

Banyan USA Surgical Mask Level 3 received FDA 510(k) clearance on 2021-09-22, under 510(k) number K211097.

Who is the listed applicant for Banyan USA Surgical Mask Level 3?

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

What is the FDA product code for Banyan USA Surgical Mask Level 3?

The FDA product code for Banyan USA Surgical Mask Level 3 is FXX.

相關臨床試驗

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。

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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