510(k) K173810 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Ventripoint Medical System Plus (VMS+)
| Applicant | Ventripoint Diagnostics , Ltd., Toronto, CA |
| Decision | Substantially Equivalent, May 14, 2018 |
| Received | Dec 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173810
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.