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FDA 510(k)

H1

K号: K222504 · 2022-11-10

决定日期2022-11-10
产品代码GCJ
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

H1 is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy America, Inc.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K222504. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the H1?

H1 is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K222504.

When did H1 receive FDA 510(k) clearance?

H1 received FDA 510(k) clearance on 2022-11-10, under 510(k) number K222504.

Who is the listed applicant for H1?

The FDA 510(k) record lists Karl Storz Endoscopy America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for H1?

The FDA product code for H1 is GCJ.

列明Karl Storz Endoscopy America, Inc.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:GCJ)

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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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。

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