ATS 5000 自动止血带仪器
K 號：K202919 · 2021-05-20
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器材摘要
ATS 5000 Automatic Tourniquet Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Mcewen and Associates Consulting , Ltd.. It received FDA 510(k) clearance on 2021-05-20 under 510(k) number K202919. The device is classified under product code KCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ATS 5000 Automatic Tourniquet Instrument?
ATS 5000 Automatic Tourniquet Instrument is a medical device that received FDA 510(k) clearance on 2021-05-20. The listed applicant is Mcewen and Associates Consulting , Ltd.. The 510(k) number is K202919.
When did ATS 5000 Automatic Tourniquet Instrument receive FDA 510(k) clearance?
ATS 5000 Automatic Tourniquet Instrument received FDA 510(k) clearance on 2021-05-20, under 510(k) number K202919.
Who is the listed applicant for ATS 5000 Automatic Tourniquet Instrument?
The FDA 510(k) record lists Mcewen and Associates Consulting , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATS 5000 Automatic Tourniquet Instrument?
The FDA product code for ATS 5000 Automatic Tourniquet Instrument is KCY.
相關臨床試驗
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相關器械（代碼：KCY）
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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