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

FDA 510(k) Number Submission Date Device Name Applicant
K240553 02/28/2024 LVivo Software Application DiA Imaging Analysis Ltd.
K240769 03/21/2024 LVivo IQS DiA Imaging Analysis Ltd.
K243235 10/10/2024 LVivo Software Application DiA Imaging Analysis Ltd.
K243331 10/24/2024 LVivo Seamless DiA Imaging Analysis Ltd.
K243862 12/16/2024 LVivo Software Application DiA Imaging Analysis Ltd.


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