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Clearmind Biomedical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230125Neuroblade SystemOctober 13, 2023
K210251ClearPath Disposable IntroducerApril 2, 2021
K201308Axonpen, Axonmonitor, Axonbox, TabletNovember 27, 2020