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FDA 510(k)

OTSCneo 系统套装 (100.03n-14n, 100.27n-31n)

K号: K251562 · 2025-12-18

决定日期2025-12-18
产品代码PKL
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

OTSCneo System Set (100.03n-14n, 100.27n-31n) 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 2025-12-18 under 510(k) number K251562. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the OTSCneo System Set (100.03n-14n, 100.27n-31n)?

OTSCneo System Set (100.03n-14n, 100.27n-31n) is a medical device that received FDA 510(k) clearance on 2025-12-18. The listed applicant is Ovesco Endoscopy AG. The 510(k) number is K251562.

When did OTSCneo System Set (100.03n-14n, 100.27n-31n) receive FDA 510(k) clearance?

OTSCneo System Set (100.03n-14n, 100.27n-31n) received FDA 510(k) clearance on 2025-12-18, under 510(k) number K251562.

Who is the listed applicant for OTSCneo System Set (100.03n-14n, 100.27n-31n)?

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 OTSCneo System Set (100.03n-14n, 100.27n-31n)?

The FDA product code for OTSCneo System Set (100.03n-14n, 100.27n-31n) is PKL.

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。

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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相关器械(代码:PKL)

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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