FDA 510(k)

多模態檢視器

K 號：K182230 · 2018-09-07

決定日期2018-09-07

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Multi Modality Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Vital Images, Inc.. It received FDA 510(k) clearance on 2018-09-07 under 510(k) number K182230. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Multi Modality Viewer?

Multi Modality Viewer is a medical device that received FDA 510(k) clearance on 2018-09-07. The listed applicant is Vital Images, Inc.. The 510(k) number is K182230.

When did Multi Modality Viewer receive FDA 510(k) clearance?

Multi Modality Viewer received FDA 510(k) clearance on 2018-09-07, under 510(k) number K182230.

Who is the listed applicant for Multi Modality Viewer?

The FDA 510(k) record lists Vital Images, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi Modality Viewer?

The FDA product code for Multi Modality Viewer is LLZ.

其他以 Vital Images, Inc. 為申請人之記錄

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相關器械（代碼：LLZ）

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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