PIVO
K 號：K190604 · 2019-05-13
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器材摘要
PIVO is the device name listed in this FDA 510(k) record. The listed applicant is Velano Vascular. It received FDA 510(k) clearance on 2019-05-13 under 510(k) number K190604. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PIVO?
PIVO is a medical device that received FDA 510(k) clearance on 2019-05-13. The listed applicant is Velano Vascular. The 510(k) number is K190604.
When did PIVO receive FDA 510(k) clearance?
PIVO received FDA 510(k) clearance on 2019-05-13, under 510(k) number K190604.
Who is the listed applicant for PIVO?
The FDA 510(k) record lists Velano Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIVO?
The FDA product code for PIVO is JKA.
相關 PubMed 文獻
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其他以 Velano Vascular 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：JKA）
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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