可攜式霧化器
K 號：K170916 · 2017-11-28
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器材摘要
Portable Nebulizer is the device name listed in this FDA 510(k) record. The listed applicant is Microbase Technology Corporation. It received FDA 510(k) clearance on 2017-11-28 under 510(k) number K170916. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Portable Nebulizer?
Portable Nebulizer is a medical device that received FDA 510(k) clearance on 2017-11-28. The listed applicant is Microbase Technology Corporation. The 510(k) number is K170916.
When did Portable Nebulizer receive FDA 510(k) clearance?
Portable Nebulizer received FDA 510(k) clearance on 2017-11-28, under 510(k) number K170916.
Who is the listed applicant for Portable Nebulizer?
The FDA 510(k) record lists Microbase Technology Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Portable Nebulizer?
The FDA product code for Portable Nebulizer is CAF.
相關臨床試驗
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其他以 Microbase Technology Corporation 為申請人之記錄
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。
相關器械（代碼：CAF）
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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