ApexMV
K 號：K182022 · 2019-03-15
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器材摘要
ApexMV is the device name listed in this FDA 510(k) record. The listed applicant is Incontrol Medical, LLC. It received FDA 510(k) clearance on 2019-03-15 under 510(k) number K182022. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常見問題
What is the ApexMV?
ApexMV is a medical device that received FDA 510(k) clearance on 2019-03-15. The listed applicant is Incontrol Medical, LLC. The 510(k) number is K182022.
When did ApexMV receive FDA 510(k) clearance?
ApexMV received FDA 510(k) clearance on 2019-03-15, under 510(k) number K182022.
Who is the listed applicant for ApexMV?
The FDA 510(k) record lists Incontrol Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ApexMV?
The FDA product code for ApexMV is KPI.
相關臨床試驗
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相關器械（代碼：KPI）
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
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