斯特劳布內血管系統
K 號：K172315 · 2018-04-12
廣告
器材摘要
Straub Endovascular System is the device name listed in this FDA 510(k) record. The listed applicant is Straub Medical AG. It received FDA 510(k) clearance on 2018-04-12 under 510(k) number K172315. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Straub Endovascular System?
Straub Endovascular System is a medical device that received FDA 510(k) clearance on 2018-04-12. The listed applicant is Straub Medical AG. The 510(k) number is K172315.
When did Straub Endovascular System receive FDA 510(k) clearance?
Straub Endovascular System received FDA 510(k) clearance on 2018-04-12, under 510(k) number K172315.
Who is the listed applicant for Straub Endovascular System?
The FDA 510(k) record lists Straub Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Straub Endovascular System?
The FDA product code for Straub Endovascular System is MCW.
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：MCW）
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。
K260244Auryon 開心術系統Eximo MedicalK250723FreedomFlow™ 軌道環形動脈內脫落術系統 (H6005/ 4Fr 3-球體配置)Cardio Flow Inc.,K250385超級精英雷射動脈內切除針SpectraneticsK242757Rotarex 銳術系統Bard Peripheral Vascular, Inc.K242947FreedomFlow™ 軌道環形動脈內切除系統Cardio Flow Inc.,K241553Auryon 腺切除导管 1.7mm; Auryon 腺切除导管 1.7mm, 水性塗層Eximo Medical, Ltd.
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