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/ Medeia, Inc.
Medeia, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K212684
BrainView QEEG Software
January 28, 2023
K192753
NeuralScan System
March 17, 2020
K191266
VitalScan ANS
January 15, 2020
K150804
QBioScan
October 19, 2015