Biotricity, Inc. is one of 571 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Biotricity, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BioFlux Device, Bioflux Software
2
Total
2
Cleared
0
Denied
Biotricity, Inc. has 2 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biotricity, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Biotricity, Inc.
2 devices