Viz ICH
K 號：K210209 · 2021-03-23
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器材摘要
Viz ICH is the device name listed in this FDA 510(k) record. The listed applicant is Viz. Ai, Inc.. It received FDA 510(k) clearance on 2021-03-23 under 510(k) number K210209. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Viz ICH?
Viz ICH is a medical device that received FDA 510(k) clearance on 2021-03-23. The listed applicant is Viz. Ai, Inc.. The 510(k) number is K210209.
When did Viz ICH receive FDA 510(k) clearance?
Viz ICH received FDA 510(k) clearance on 2021-03-23, under 510(k) number K210209.
Who is the listed applicant for Viz ICH?
The FDA 510(k) record lists Viz. Ai, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Viz ICH?
The FDA product code for Viz ICH is QAS.
其他以 Viz. Ai, Inc. 為申請人之記錄
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相關器械（代碼：QAS）
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
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。
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