FDA 510(k)

CliniCloud 非接触式体温計、モデル SPL1024

K番号: K161325 · 2016-06-22

決定日2016-06-22

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

CliniCloud Non-contact Thermometer, Model SPL1024 is the device name listed in this FDA 510(k) record. The listed applicant is Stethocloud Pty.Ltd (Clinicloud). It received FDA 510(k) clearance on 2016-06-22 under 510(k) number K161325. 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 CliniCloud Non-contact Thermometer, Model SPL1024?

CliniCloud Non-contact Thermometer, Model SPL1024 is a medical device that received FDA 510(k) clearance on 2016-06-22. The listed applicant is Stethocloud Pty.Ltd (Clinicloud). The 510(k) number is K161325.

When did CliniCloud Non-contact Thermometer, Model SPL1024 receive FDA 510(k) clearance?

CliniCloud Non-contact Thermometer, Model SPL1024 received FDA 510(k) clearance on 2016-06-22, under 510(k) number K161325.

Who is the listed applicant for CliniCloud Non-contact Thermometer, Model SPL1024?

The FDA 510(k) record lists Stethocloud Pty.Ltd (Clinicloud) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CliniCloud Non-contact Thermometer, Model SPL1024?

The FDA product code for CliniCloud Non-contact Thermometer, Model SPL1024 is FLL.

申請者としてStethocloud Pty.Ltd (Clinicloud)を記載するその他の記録

K173448クリニクラウドステトスコープ

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