快速ICH
K 號：K193087 · 2020-03-31
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器材摘要
Rapid ICH is the device name listed in this FDA 510(k) record. The listed applicant is Ischemaview Incorporated. It received FDA 510(k) clearance on 2020-03-31 under 510(k) number K193087. 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 Rapid ICH?
Rapid ICH is a medical device that received FDA 510(k) clearance on 2020-03-31. The listed applicant is Ischemaview Incorporated. The 510(k) number is K193087.
When did Rapid ICH receive FDA 510(k) clearance?
Rapid ICH received FDA 510(k) clearance on 2020-03-31, under 510(k) number K193087.
Who is the listed applicant for Rapid ICH?
The FDA 510(k) record lists Ischemaview Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rapid ICH?
The FDA product code for Rapid ICH is QAS.
相關臨床試驗
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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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