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FDA 510(k)

Amazing+

K号: K212586 · 2022-02-17

决定日期2022-02-17
产品代码LZA
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

Amazing+ is the device name listed in this FDA 510(k) record. The listed applicant is Amazing Rubber Products Pvt, Ltd.. It received FDA 510(k) clearance on 2022-02-17 under 510(k) number K212586. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Amazing+?

Amazing+ is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Amazing Rubber Products Pvt, Ltd.. The 510(k) number is K212586.

When did Amazing+ receive FDA 510(k) clearance?

Amazing+ received FDA 510(k) clearance on 2022-02-17, under 510(k) number K212586.

Who is the listed applicant for Amazing+?

The FDA 510(k) record lists Amazing Rubber Products Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Amazing+?

The FDA product code for Amazing+ is LZA.

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Amazing Rubber Products Pvt, Ltd.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:LZA)

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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