FDA 510(k), K200232, LVivo Software Application

510(K) Number: K200232
Device Name: LVivo Software Application
Manufacturer: DiA Imaging Analysis Ltd
Device Classification Name: Automated Radiological Image Processing Software
Regulation Number: 892.2050
Classification Product Code: QIH
Date Received: 01/30/2020
Decision Date: 06/23/2020
Regulation Medical Specialty: Radiology

260 pages (1,162 of 1,422 pages are fully redacted)