FDA 510(k)

Philips VSC-MEDlib

K号: K242001 · 2025-04-04

申请人Philips Medical Systems Nederland B.V.

决定日期2025-04-04

产品代码BZQ

咨询委员会AN 请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。

决定实质等同

器械摘要

Philips VSC-MEDlib is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2025-04-04 under 510(k) number K242001. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Philips VSC-MEDlib?

Philips VSC-MEDlib is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K242001.

When did Philips VSC-MEDlib receive FDA 510(k) clearance?

Philips VSC-MEDlib received FDA 510(k) clearance on 2025-04-04, under 510(k) number K242001.

Who is the listed applicant for Philips VSC-MEDlib?

FDA 510(k)记录中列出Philips Medical Systems Nederland B.V.为申请人。这本身并不足以确定该设备的制造商。

What is the FDA product code for Philips VSC-MEDlib?

The FDA product code for Philips VSC-MEDlib is BZQ.

列明Philips Medical Systems Nederland B.V.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。

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