Apinator
K 號：K160123 · 2016-07-12
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器材摘要
Apinator is the device name listed in this FDA 510(k) record. The listed applicant is Allen J. Moses, Dds, Ltd.. It received FDA 510(k) clearance on 2016-07-12 under 510(k) number K160123. 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 Apinator?
Apinator is a medical device that received FDA 510(k) clearance on 2016-07-12. The listed applicant is Allen J. Moses, Dds, Ltd.. The 510(k) number is K160123.
When did Apinator receive FDA 510(k) clearance?
Apinator received FDA 510(k) clearance on 2016-07-12, under 510(k) number K160123.
Who is the listed applicant for Apinator?
The FDA 510(k) record lists Allen J. Moses, Dds, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apinator?
The FDA product code for Apinator is LRK.
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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。
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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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