口袋噴霧器
K 號:K142541 · 2016-01-22
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器材摘要
POCKET NEB is the device name listed in this FDA 510(k) record. The listed applicant is Microvaper Devices. It received FDA 510(k) clearance on 2016-01-22 under 510(k) number K142541. 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 POCKET NEB?
POCKET NEB is a medical device that received FDA 510(k) clearance on 2016-01-22. The listed applicant is Microvaper Devices. The 510(k) number is K142541.
When did POCKET NEB receive FDA 510(k) clearance?
POCKET NEB received FDA 510(k) clearance on 2016-01-22, under 510(k) number K142541.
Who is the listed applicant for POCKET NEB?
The FDA 510(k) record lists Microvaper Devices as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POCKET NEB?
The FDA product code for POCKET NEB is CAF.
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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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