FDA 510(k) Applications Submitted by Vysioneer Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K203235 11/03/2020 VBrain Vysioneer Inc.
K212116 07/07/2021 VBrain-OAR Vysioneer Inc.
K213628 11/17/2021 VBrain Vysioneer Inc.


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