FLEX 腹腔內預處理系統
K 號：K202187 · 2020-09-11
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器材摘要
FLEX Vessel Prep System is the device name listed in this FDA 510(k) record. The listed applicant is Venturemed Group, Inc.. It received FDA 510(k) clearance on 2020-09-11 under 510(k) number K202187. The device is classified under product code PNO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the FLEX Vessel Prep System?
FLEX Vessel Prep System is a medical device that received FDA 510(k) clearance on 2020-09-11. The listed applicant is Venturemed Group, Inc.. The 510(k) number is K202187.
When did FLEX Vessel Prep System receive FDA 510(k) clearance?
FLEX Vessel Prep System received FDA 510(k) clearance on 2020-09-11, under 510(k) number K202187.
Who is the listed applicant for FLEX Vessel Prep System?
The FDA 510(k) record lists Venturemed Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEX Vessel Prep System?
The FDA product code for FLEX Vessel Prep System is PNO.
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相關器械（代碼：PNO）
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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