FDA 510(k)

Fever Scout

K号: K181013 · 2018-08-21

决定日期2018-08-21

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

Fever Scout is the device name listed in this FDA 510(k) record. The listed applicant is VivaLNK, Inc.. It received FDA 510(k) clearance on 2018-08-21 under 510(k) number K181013. 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 Fever Scout?

Fever Scout is a medical device that received FDA 510(k) clearance on 2018-08-21. The listed applicant is VivaLNK, Inc.. The 510(k) number is K181013.

When did Fever Scout receive FDA 510(k) clearance?

Fever Scout received FDA 510(k) clearance on 2018-08-21, under 510(k) number K181013.

Who is the listed applicant for Fever Scout?

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

What is the FDA product code for Fever Scout?

The FDA product code for Fever Scout is FLL.

列明VivaLNK, 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。

K191870VV330连续心电图平台，VivaLNK粘性贴片 K162137Fever Scout™ 连续监测体温计

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。

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官方来源

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