鼻塞停和止血停
K 號：K183622 · 2019-12-02
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器材摘要
NasalCEASE and BleedCEASE is the device name listed in this FDA 510(k) record. The listed applicant is Les Laboratoires Brothier S.A.. It received FDA 510(k) clearance on 2019-12-02 under 510(k) number K183622. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.
常見問題
What is the NasalCEASE and BleedCEASE?
NasalCEASE and BleedCEASE is a medical device that received FDA 510(k) clearance on 2019-12-02. The listed applicant is Les Laboratoires Brothier S.A.. The 510(k) number is K183622.
When did NasalCEASE and BleedCEASE receive FDA 510(k) clearance?
NasalCEASE and BleedCEASE received FDA 510(k) clearance on 2019-12-02, under 510(k) number K183622.
Who is the listed applicant for NasalCEASE and BleedCEASE?
The FDA 510(k) record lists Les Laboratoires Brothier S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NasalCEASE and BleedCEASE?
The FDA product code for NasalCEASE and BleedCEASE is QSY.
相關臨床試驗
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相關器械（代碼：QSY）
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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