FDA 510(k), K211798, Cleaner Plus Thrombectomy System

FDA 510(k), K211798, Cleaner Plus Thrombectomy System

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510(K) Number: K211798
Device Name: Cleaner Plus Thrombectomy System
Manufacturer: Ana Jimenez-Hughes
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: QEW
Classification Product Code: 06/10/2021
Date Received: 02/24/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular

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