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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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