510(k) K172311 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
BioFlux Device
| Applicant | Biotricity, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Aug 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172311
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.