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FDA 510(k)

Phoenix数字体温计

K号: K201032 · 2021-10-29

决定日期2021-10-29
产品代码FLL
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

Phoenix Digital Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. It received FDA 510(k) clearance on 2021-10-29 under 510(k) number K201032. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Phoenix Digital Thermometer?

Phoenix Digital Thermometer is a medical device that received FDA 510(k) clearance on 2021-10-29. The listed applicant is Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. The 510(k) number is K201032.

When did Phoenix Digital Thermometer receive FDA 510(k) clearance?

Phoenix Digital Thermometer received FDA 510(k) clearance on 2021-10-29, under 510(k) number K201032.

Who is the listed applicant for Phoenix Digital Thermometer?

The FDA 510(k) record lists Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Phoenix Digital Thermometer?

The FDA product code for Phoenix Digital Thermometer is FLL.

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Phoenix Innovative Healthcare Manufacturers 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:FLL)

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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