藍普羅
K 號：K162192 · 2016-12-15
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器材摘要
BluePro is the device name listed in this FDA 510(k) record. The listed applicant is Bluesom. It received FDA 510(k) clearance on 2016-12-15 under 510(k) number K162192. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BluePro?
BluePro is a medical device that received FDA 510(k) clearance on 2016-12-15. The listed applicant is Bluesom. The 510(k) number is K162192.
When did BluePro receive FDA 510(k) clearance?
BluePro received FDA 510(k) clearance on 2016-12-15, under 510(k) number K162192.
Who is the listed applicant for BluePro?
The FDA 510(k) record lists Bluesom as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BluePro?
The FDA product code for BluePro is LRK.
相關臨床試驗
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相關器械（代碼：LRK）
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。
K262104防鼾口器（L09-BB、L09-PP、L09-TB、L09-BT、L09-TP、L09-PT、L09-TT）Ram.Shaw Pte., Ltd.K261912SnøreNegatØr
注意：此翻譯僅根據給定的文本進行，並未考慮到專業醫療設備規範文本的完整性和細節。在實際應用中，請確保翻譯符合相關醫療設備規範要求。DnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® 阻止打鼾設備Endeavor Commerce, LLCK261134Dormiva 防打鼾口器Koncept Innovators, Inc.K252942ShaeferH
醫療設備規範文本翻譯：
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注意：公司名稱、產品名稱、FDA、510(k)、PMA、NCT、PMID、識別碼和網址等均未進行翻譯，以保留原文。Shaeferh, LLC
官方來源
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