FDA 510(k)

LVivo 軟體應用程序

K 號：K200232 · 2020-06-23

決定日期2020-06-23

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

LVivo Software Application is the device name listed in this FDA 510(k) record. The listed applicant is Dia Imaging Analysis, Ltd.. It received FDA 510(k) clearance on 2020-06-23 under 510(k) number K200232. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LVivo Software Application?

LVivo Software Application is a medical device that received FDA 510(k) clearance on 2020-06-23. The listed applicant is Dia Imaging Analysis, Ltd.. The 510(k) number is K200232.

When did LVivo Software Application receive FDA 510(k) clearance?

LVivo Software Application received FDA 510(k) clearance on 2020-06-23, under 510(k) number K200232.

Who is the listed applicant for LVivo Software Application?

The FDA 510(k) record lists Dia Imaging Analysis, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LVivo Software Application?

The FDA product code for LVivo Software Application is QIH.

其他以 Dia Imaging Analysis, Ltd. 為申請人之記錄

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相關器械（代碼：QIH）

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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