BioFlux Device— 510(k) K172311

Substantially Equivalent

Biotricity, Inc.

FDA 510(k) clearance K172311 for BioFlux Device, Substantially Equivalent on 2017-12-15. Applicant: Biotricity, Inc..

Clearance details

Applicant: Biotricity, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 2017-08-01
Decision date: 2017-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redwood City, CA, US

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