FDA 510(k)

インフラレッドノンタッチ体温計、モデルACT8100

K番号: K162509 · 2017-03-10

決定日2017-03-10

製品コードFLL

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定大幅同等

医療機器の概要

Infrared Non-contact Thermometer, Model ACT8100 is the device name listed in this FDA 510(k) record. The listed applicant is Easywell Biomedicals, Inc.. It received FDA 510(k) clearance on 2017-03-10 under 510(k) number K162509. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Infrared Non-contact Thermometer, Model ACT8100?

Infrared Non-contact Thermometer, Model ACT8100 is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is Easywell Biomedicals, Inc.. The 510(k) number is K162509.

When did Infrared Non-contact Thermometer, Model ACT8100 receive FDA 510(k) clearance?

Infrared Non-contact Thermometer, Model ACT8100 received FDA 510(k) clearance on 2017-03-10, under 510(k) number K162509.

Who is the listed applicant for Infrared Non-contact Thermometer, Model ACT8100?

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

What is the FDA product code for Infrared Non-contact Thermometer, Model ACT8100?

The FDA product code for Infrared Non-contact Thermometer, Model ACT8100 is FLL.

申請者としてEasywell Biomedicals, Inc.を記載するその他の記録

K163166EASYWELL TENSシステム TENSおよびヒート、EASYWELL TENSシステム TENSのみ

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