FDA 510(k)

RadiForce MX317W-PA

K号: K242545 · 2025-05-23

决定日期2025-05-23

产品代码PZZ

咨询委员会PA 请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。

决定实质等同

器械摘要

RadiForce MX317W-PA is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Corporation. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K242545. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the RadiForce MX317W-PA?

RadiForce MX317W-PA is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Eizo Corporation. The 510(k) number is K242545.

When did RadiForce MX317W-PA receive FDA 510(k) clearance?

RadiForce MX317W-PA received FDA 510(k) clearance on 2025-05-23, under 510(k) number K242545.

Who is the listed applicant for RadiForce MX317W-PA?

FDA 510(k)记录中列出Eizo Corporation为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for RadiForce MX317W-PA?

The FDA product code for RadiForce MX317W-PA is PZZ.

列明Eizo Corporation为申报人的其他记录

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。

K262397CuratOR EX2742 K262783RadiForce MX247W K252030RadiForce GX570; RadiForce GX570-AR K243221RadiForce RX570; RadiForce RX570-AR K241441RadiForce RX670; RadiForce RX670-AR K233465RadiForce MX317W

查看所有 23 个设备 →

官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。