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FDA 510(k)

Aixplorer & Aixplorer Ultimate 超聲診斷系統

K 號:K173021 · 2018-01-09

決定日期2018-01-09
產品代碼IYN
諮詢委員會RA
決定相當於

器材摘要

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is the device name listed in this FDA 510(k) record. The listed applicant is Supersonic Imagine. It received FDA 510(k) clearance on 2018-01-09 under 510(k) number K173021. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is a medical device that received FDA 510(k) clearance on 2018-01-09. The listed applicant is Supersonic Imagine. The 510(k) number is K173021.

When did Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems receive FDA 510(k) clearance?

Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems received FDA 510(k) clearance on 2018-01-09, under 510(k) number K173021.

Who is the listed applicant for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

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

What is the FDA product code for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems?

The FDA product code for Aixplorer & Aixplorer Ultimate Ultrasound Diagnostic Systems is IYN.

相關臨床試驗

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。

其他以 Supersonic Imagine 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:IYN)

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。

官方來源

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