快速血管阻塞（快速VO）
K 號：K261085 · 2026-07-13
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器材摘要
Rapid Vessel Occlusion (Rapid VO) is the device name listed in this FDA 510(k) record. The listed applicant is iSchemaview. It received FDA 510(k) clearance on 2026-07-13 under 510(k) number K261085. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Rapid Vessel Occlusion (Rapid VO)?
Rapid Vessel Occlusion (Rapid VO) is a medical device that received FDA 510(k) clearance on 2026-07-13. The listed applicant is iSchemaview. The 510(k) number is K261085.
When did Rapid Vessel Occlusion (Rapid VO) receive FDA 510(k) clearance?
Rapid Vessel Occlusion (Rapid VO) received FDA 510(k) clearance on 2026-07-13, under 510(k) number K261085.
Who is the listed applicant for Rapid Vessel Occlusion (Rapid VO)?
The FDA 510(k) record lists iSchemaview as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rapid Vessel Occlusion (Rapid VO)?
The FDA product code for Rapid Vessel Occlusion (Rapid VO) is QAS.
相關臨床試驗
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其他以 iSchemaview 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：QAS）
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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