奧米尼亞醫療VBR
K 號：K172323 · 2017-10-26
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器材摘要
Omnia Medical VBR is the device name listed in this FDA 510(k) record. The listed applicant is Omnia Medical, LLC. It received FDA 510(k) clearance on 2017-10-26 under 510(k) number K172323. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Omnia Medical VBR?
Omnia Medical VBR is a medical device that received FDA 510(k) clearance on 2017-10-26. The listed applicant is Omnia Medical, LLC. The 510(k) number is K172323.
When did Omnia Medical VBR receive FDA 510(k) clearance?
Omnia Medical VBR received FDA 510(k) clearance on 2017-10-26, under 510(k) number K172323.
Who is the listed applicant for Omnia Medical VBR?
The FDA 510(k) record lists Omnia Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Omnia Medical VBR?
The FDA product code for Omnia Medical VBR is MQP.
相關臨床試驗
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其他以 Omnia Medical, LLC 為申請人之記錄
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。
相關器械（代碼：MQP）
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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