510(k) K172142 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
FibroScan 430 Mini+
| Applicant | Echosens, Paris, FR |
| Decision | Substantially Equivalent, Sep 13, 2017 |
| Received | Jul 17, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172142
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.