FDA 510(k)

升級套件 MR GUI PRO，MrJ 3300 Plus

K 號：K192690 · 2019-10-24

決定日期2019-10-24

產品代碼LNH

諮詢委員會RA

決定相當於

器材摘要

Upgrade Kit MR GUI PRO, MrJ 3300 Plus is the device name listed in this FDA 510(k) record. The listed applicant is Asg Superconductors S.P.A.. It received FDA 510(k) clearance on 2019-10-24 under 510(k) number K192690. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Upgrade Kit MR GUI PRO, MrJ 3300 Plus?

Upgrade Kit MR GUI PRO, MrJ 3300 Plus is a medical device that received FDA 510(k) clearance on 2019-10-24. The listed applicant is Asg Superconductors S.P.A.. The 510(k) number is K192690.

When did Upgrade Kit MR GUI PRO, MrJ 3300 Plus receive FDA 510(k) clearance?

Upgrade Kit MR GUI PRO, MrJ 3300 Plus received FDA 510(k) clearance on 2019-10-24, under 510(k) number K192690.

Who is the listed applicant for Upgrade Kit MR GUI PRO, MrJ 3300 Plus?

The FDA 510(k) record lists Asg Superconductors S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Upgrade Kit MR GUI PRO, MrJ 3300 Plus?

The FDA product code for Upgrade Kit MR GUI PRO, MrJ 3300 Plus is LNH.

其他以 Asg Superconductors S.P.A. 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。

K242258MROpen Evo (03-2000-00)；MROpen Evo (03-4000-00)K193116MRopen EVO K190524MRopen 0.5 T

相關器械（代碼：LNH）

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。

K261283APERTO Lucent MRI 系統Fujifilm Corporation K261758擁抱視覺新生兒MRI系統Aspect Imaging, Ltd.K260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® 輕便式磁共振成像® 系統Hyperfine, Inc.K254250MagicScan-1.5，綠色MR寧靜1.5TXingaoyi Medical Equipment Co.,Ltd K253808空氣偵探 DLGE Medical Systems

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。