SQuEEZ 軟體
K 號：K201250 · 2020-12-18
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器材摘要
SQuEEZ Software is the device name listed in this FDA 510(k) record. The listed applicant is Cardiowise, Inc.. It received FDA 510(k) clearance on 2020-12-18 under 510(k) number K201250. 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 SQuEEZ Software?
SQuEEZ Software is a medical device that received FDA 510(k) clearance on 2020-12-18. The listed applicant is Cardiowise, Inc.. The 510(k) number is K201250.
When did SQuEEZ Software receive FDA 510(k) clearance?
SQuEEZ Software received FDA 510(k) clearance on 2020-12-18, under 510(k) number K201250.
Who is the listed applicant for SQuEEZ Software?
The FDA 510(k) record lists Cardiowise, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SQuEEZ Software?
The FDA product code for SQuEEZ 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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