broncholab
K 號：K191550 · 2020-03-04
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器材摘要
Broncholab is the device name listed in this FDA 510(k) record. The listed applicant is Fluidda, Inc.. It received FDA 510(k) clearance on 2020-03-04 under 510(k) number K191550. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Broncholab?
Broncholab is a medical device that received FDA 510(k) clearance on 2020-03-04. The listed applicant is Fluidda, Inc.. The 510(k) number is K191550.
When did Broncholab receive FDA 510(k) clearance?
Broncholab received FDA 510(k) clearance on 2020-03-04, under 510(k) number K191550.
Who is the listed applicant for Broncholab?
The FDA 510(k) record lists Fluidda, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Broncholab?
The FDA product code for Broncholab is JAK.
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相關器械（代碼：JAK）
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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