FDA 510(k)

最新醫用口罩

K 號：K214035 · 2022-09-13

決定日期2022-09-13

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

LAITEST Medical Face Mask is the device name listed in this FDA 510(k) record. The listed applicant is R&R Medical Corporation, Ltd.. It received FDA 510(k) clearance on 2022-09-13 under 510(k) number K214035. 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 LAITEST Medical Face Mask?

LAITEST Medical Face Mask is a medical device that received FDA 510(k) clearance on 2022-09-13. The listed applicant is R&R Medical Corporation, Ltd.. The 510(k) number is K214035.

When did LAITEST Medical Face Mask receive FDA 510(k) clearance?

LAITEST Medical Face Mask received FDA 510(k) clearance on 2022-09-13, under 510(k) number K214035.

Who is the listed applicant for LAITEST Medical Face Mask?

The FDA 510(k) record lists R&R Medical Corporation, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAITEST Medical Face Mask?

The FDA product code for LAITEST Medical Face Mask is FXX.

其他以 R&R Medical Corporation, Ltd. 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。

K220226X-Y 滑潤膠

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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