QyScore 軟體
K 號：K192531 · 2019-12-13
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器材摘要
QyScore Software is the device name listed in this FDA 510(k) record. The listed applicant is Qynapse. It received FDA 510(k) clearance on 2019-12-13 under 510(k) number K192531. 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 QyScore Software?
QyScore Software is a medical device that received FDA 510(k) clearance on 2019-12-13. The listed applicant is Qynapse. The 510(k) number is K192531.
When did QyScore Software receive FDA 510(k) clearance?
QyScore Software received FDA 510(k) clearance on 2019-12-13, under 510(k) number K192531.
Who is the listed applicant for QyScore Software?
The FDA 510(k) record lists Qynapse as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QyScore Software?
The FDA product code for QyScore Software is LLZ.
相關臨床試驗
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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。
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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