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FDA 510(k)

nextaro® va,15mm,5µm

K号: K241976 · 2024-09-06

决定日期2024-09-06
产品代码LHI
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

nextaro® va, 15mm, 5µm is the device name listed in this FDA 510(k) record. The listed applicant is Sfm Medical Devices GmbH. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K241976. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the nextaro® va, 15mm, 5µm?

nextaro® va, 15mm, 5µm is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Sfm Medical Devices GmbH. The 510(k) number is K241976.

When did nextaro® va, 15mm, 5µm receive FDA 510(k) clearance?

nextaro® va, 15mm, 5µm received FDA 510(k) clearance on 2024-09-06, under 510(k) number K241976.

Who is the listed applicant for nextaro® va, 15mm, 5µm?

The FDA 510(k) record lists Sfm Medical Devices GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for nextaro® va, 15mm, 5µm?

The FDA product code for nextaro® va, 15mm, 5µm is LHI.

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Sfm Medical Devices GmbH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。

相关器械(代码:LHI)

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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