托羅88超粗內腔導管
K 號：K252297 · 2026-01-16
廣告
器材摘要
Toro 88 Superbore Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Toro Neurovascular, Inc.. It received FDA 510(k) clearance on 2026-01-16 under 510(k) number K252297. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Toro 88 Superbore Catheter?
Toro 88 Superbore Catheter is a medical device that received FDA 510(k) clearance on 2026-01-16. The listed applicant is Toro Neurovascular, Inc.. The 510(k) number is K252297.
When did Toro 88 Superbore Catheter receive FDA 510(k) clearance?
Toro 88 Superbore Catheter received FDA 510(k) clearance on 2026-01-16, under 510(k) number K252297.
Who is the listed applicant for Toro 88 Superbore Catheter?
The FDA 510(k) record lists Toro Neurovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Toro 88 Superbore Catheter?
The FDA product code for Toro 88 Superbore Catheter is QJP.
相關臨床試驗
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：QJP）
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。
廣告