CONNEQT 脈搏
K 號：K221742 · 2023-04-21
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器材摘要
CONNEQT PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Atcor Medical. It received FDA 510(k) clearance on 2023-04-21 under 510(k) number K221742. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CONNEQT PULSE?
CONNEQT PULSE is a medical device that received FDA 510(k) clearance on 2023-04-21. The listed applicant is Atcor Medical. The 510(k) number is K221742.
When did CONNEQT PULSE receive FDA 510(k) clearance?
CONNEQT PULSE received FDA 510(k) clearance on 2023-04-21, under 510(k) number K221742.
Who is the listed applicant for CONNEQT PULSE?
The FDA 510(k) record lists Atcor Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONNEQT PULSE?
The FDA product code for CONNEQT PULSE is DXN.
相關臨床試驗
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相關器械（代碼：DXN）
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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官方來源
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