Luco雙模態OSA設備
K 號：K160477 · 2016-07-29
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器材摘要
The Luco Hybrid OSA Appliance is the device name listed in this FDA 510(k) record. The listed applicant is Luco Hybrid Osa Appliance, Inc.. It received FDA 510(k) clearance on 2016-07-29 under 510(k) number K160477. The device is classified under product code OCO. FDA Decision: Substantially Equivalent.
常見問題
What is the The Luco Hybrid OSA Appliance?
The Luco Hybrid OSA Appliance is a medical device that received FDA 510(k) clearance on 2016-07-29. The listed applicant is Luco Hybrid Osa Appliance, Inc.. The 510(k) number is K160477.
When did The Luco Hybrid OSA Appliance receive FDA 510(k) clearance?
The Luco Hybrid OSA Appliance received FDA 510(k) clearance on 2016-07-29, under 510(k) number K160477.
Who is the listed applicant for The Luco Hybrid OSA Appliance?
The FDA 510(k) record lists Luco Hybrid Osa Appliance, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for The Luco Hybrid OSA Appliance?
The FDA product code for The Luco Hybrid OSA Appliance is OCO.
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相關器械（代碼：OCO）
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。
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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