電動鼻吸器
K 號：K222547 · 2022-10-20
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器材摘要
Electric nasal aspirator is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Xinlianfeng Technology Co.,Ltd. It received FDA 510(k) clearance on 2022-10-20 under 510(k) number K222547. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Electric nasal aspirator?
Electric nasal aspirator is a medical device that received FDA 510(k) clearance on 2022-10-20. The listed applicant is Shenzhen Xinlianfeng Technology Co.,Ltd. The 510(k) number is K222547.
When did Electric nasal aspirator receive FDA 510(k) clearance?
Electric nasal aspirator received FDA 510(k) clearance on 2022-10-20, under 510(k) number K222547.
Who is the listed applicant for Electric nasal aspirator?
The FDA 510(k) record lists Shenzhen Xinlianfeng Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric nasal aspirator?
The FDA product code for Electric nasal aspirator is BTA.
相關臨床試驗
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相關器械（代碼：BTA）
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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