FDA 510(k) Applications Submitted by DiA Imaging Analysis Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K210053 01/08/2021 LVivo Software Application DiA Imaging Analysis Ltd
K200232 01/30/2020 LVivo Software Application DiA Imaging Analysis Ltd
K212466 08/06/2021 LVivo Seamless DiA Imaging Analysis Ltd
K202546 09/02/2020 LVivo Seamless DiA Imaging Analysis Ltd
K222970 09/27/2022 LVivo IQS DiA Imaging Analysis Ltd


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact