FDA 510(k)

ArgoCap (200.52)

K号: K242586 · 2025-05-22

决定日期2025-05-22

产品代码OCX

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决定实质等同

器械摘要

ArgoCap (200.52) is the device name listed in this FDA 510(k) record. The listed applicant is Ovesco Endoscopy AG. It received FDA 510(k) clearance on 2025-05-22 under 510(k) number K242586. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ArgoCap (200.52)?

ArgoCap (200.52) is a medical device that received FDA 510(k) clearance on 2025-05-22. The listed applicant is Ovesco Endoscopy AG. The 510(k) number is K242586.

When did ArgoCap (200.52) receive FDA 510(k) clearance?

ArgoCap (200.52) received FDA 510(k) clearance on 2025-05-22, under 510(k) number K242586.

Who is the listed applicant for ArgoCap (200.52)?

FDA 510(k)记录显示Ovesco Endoscopy AG为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for ArgoCap (200.52)?

The FDA product code for ArgoCap (200.52) is OCX.

列明Ovesco Endoscopy AG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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官方来源

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