FDA 510(k)

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K 號：K181013 · 2018-08-21

決定日期2018-08-21

產品代碼FLL

諮詢委員會醫療設備規範文本翻譯如下： HO 注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。

決定相當於

器材摘要

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.

常見問題

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.

其他以 VivaLNK, Inc. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K191870VV330 持續心電圖平台，VivaLNK 粘貼片 K162137Fever Scout™ 持續監測式體溫計

相關器械（代碼：FLL）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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