Acare 吸引單位
K 號：K182950 · 2019-08-23
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器材摘要
Acare Suction Unit is the device name listed in this FDA 510(k) record. The listed applicant is Acare Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-08-23 under 510(k) number K182950. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Acare Suction Unit?
Acare Suction Unit is a medical device that received FDA 510(k) clearance on 2019-08-23. The listed applicant is Acare Technology Co., Ltd.. The 510(k) number is K182950.
When did Acare Suction Unit receive FDA 510(k) clearance?
Acare Suction Unit received FDA 510(k) clearance on 2019-08-23, under 510(k) number K182950.
Who is the listed applicant for Acare Suction Unit?
The FDA 510(k) record lists Acare Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acare Suction Unit?
The FDA product code for Acare Suction Unit is JCX.
相關臨床試驗
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相關器械（代碼：JCX）
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
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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