FDA 510(k)

布蘭德 BFH175 紅外線額頭溫度計

K 號：K181015 · 2018-07-18

申請人Kaz USA, Inc., A Helen of Troy Company

決定日期2018-07-18

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

Braun BFH175 Infrared Forehead Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Kaz USA, Inc., A Helen of Troy Company. It received FDA 510(k) clearance on 2018-07-18 under 510(k) number K181015. 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 Braun BFH175 Infrared Forehead Thermometer?

Braun BFH175 Infrared Forehead Thermometer is a medical device that received FDA 510(k) clearance on 2018-07-18. The listed applicant is Kaz USA, Inc., A Helen of Troy Company. The 510(k) number is K181015.

When did Braun BFH175 Infrared Forehead Thermometer receive FDA 510(k) clearance?

Braun BFH175 Infrared Forehead Thermometer received FDA 510(k) clearance on 2018-07-18, under 510(k) number K181015.

Who is the listed applicant for Braun BFH175 Infrared Forehead Thermometer?

The FDA 510(k) record lists Kaz USA, Inc., A Helen of Troy Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Braun BFH175 Infrared Forehead Thermometer?

The FDA product code for Braun BFH175 Infrared Forehead Thermometer is FLL.

其他以 Kaz USA, Inc., A Helen of Troy Company 為申請人之記錄

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相關器械（代碼：FLL）

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