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Biotricity, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K222017
Biotres
July 28, 2022
K211709
Biotres
January 19, 2022
K201040
Bioflux Software II
July 29, 2020
K172311
BioFlux Device
December 15, 2017
K162571
Bioflux Software
October 13, 2016