FDA 510(k)

雅典娜 GTX 裝置管理套件（ADMS）軟體

K 號：K173203 · 2018-03-14

決定日期2018-03-14

產品代碼MSX

諮詢委員會履歷

決定相當於

器材摘要

Athena GTX Device Management Suite (ADMS) Software is the device name listed in this FDA 510(k) record. The listed applicant is Athena Gtx. It received FDA 510(k) clearance on 2018-03-14 under 510(k) number K173203. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Athena GTX Device Management Suite (ADMS) Software?

Athena GTX Device Management Suite (ADMS) Software is a medical device that received FDA 510(k) clearance on 2018-03-14. The listed applicant is Athena Gtx. The 510(k) number is K173203.

When did Athena GTX Device Management Suite (ADMS) Software receive FDA 510(k) clearance?

Athena GTX Device Management Suite (ADMS) Software received FDA 510(k) clearance on 2018-03-14, under 510(k) number K173203.

Who is the listed applicant for Athena GTX Device Management Suite (ADMS) Software?

The FDA 510(k) record lists Athena Gtx as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Athena GTX Device Management Suite (ADMS) Software?

The FDA product code for Athena GTX Device Management Suite (ADMS) Software is MSX.

其他以 Athena Gtx 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。

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相關器械（代碼：MSX）

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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