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FDA 510(k)

CAREWE 外科口罩型号 N001-AW,N002-AW 和 N003-AW

K号: K203078 · 2022-08-19

决定日期2022-08-19
产品代码FXX
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Tianchang Industrial Co., Ltd.. It received FDA 510(k) clearance on 2022-08-19 under 510(k) number K203078. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW?

CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW is a medical device that received FDA 510(k) clearance on 2022-08-19. The listed applicant is Huizhou Tianchang Industrial Co., Ltd.. The 510(k) number is K203078.

When did CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW receive FDA 510(k) clearance?

CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW received FDA 510(k) clearance on 2022-08-19, under 510(k) number K203078.

Who is the listed applicant for CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW?

The FDA 510(k) record lists Huizhou Tianchang Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW?

The FDA product code for CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW is FXX.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

相关器械(代码:FXX)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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