FDA 510(k)

我的QA iON

K 號：K201798 · 2020-07-17

決定日期2020-07-17

產品代碼LHN

諮詢委員會RA

決定相當於

器材摘要

myQA iON is the device name listed in this FDA 510(k) record. The listed applicant is Iba Dosimetry GmbH. It received FDA 510(k) clearance on 2020-07-17 under 510(k) number K201798. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the myQA iON?

myQA iON is a medical device that received FDA 510(k) clearance on 2020-07-17. The listed applicant is Iba Dosimetry GmbH. The 510(k) number is K201798.

When did myQA iON receive FDA 510(k) clearance?

myQA iON received FDA 510(k) clearance on 2020-07-17, under 510(k) number K201798.

Who is the listed applicant for myQA iON?

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

What is the FDA product code for myQA iON?

The FDA product code for myQA iON is LHN.

其他以 Iba Dosimetry GmbH 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。

K191821藍幻影PT

相關器械（代碼：LHN）

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。

K260597VIRTUE QAProNova Solutions K260174PROBEAT-CRHitachi High-Tech Corp.K252815ProBeam 360 陽子治療系統 v3.0Varian Medical Systems, Inc.K253406S250-FIT 酸子束放射治療設備（S250-FIT）Mevion Medical Systems, Inc.K250986S250-FIT 酸子束放射治療設備（S250-FIT）Mevion Medical Systems, Inc.K243900eMotus 呼吸動態管理系統Empnia, Inc.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。