FDA 510(k)

VDT985US 薇克智慧溫度計

K 號：K152975 · 2016-03-23

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

決定日期2016-03-23

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

VDT985US Vicks SmartTemp 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 2016-03-23 under 510(k) number K152975. 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 VDT985US Vicks SmartTemp Thermometer?

VDT985US Vicks SmartTemp Thermometer is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Kaz USA, Inc., A Helen of Troy Company. The 510(k) number is K152975.

When did VDT985US Vicks SmartTemp Thermometer receive FDA 510(k) clearance?

VDT985US Vicks SmartTemp Thermometer received FDA 510(k) clearance on 2016-03-23, under 510(k) number K152975.

Who is the listed applicant for VDT985US Vicks SmartTemp 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 VDT985US Vicks SmartTemp Thermometer?

The FDA product code for VDT985US Vicks SmartTemp 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）

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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