510(k) K150580 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
UltraVision 2 Diagnostic Ultrasound System
| Applicant | Winprobe Corporation, Palm Beach Gradens FL, US |
| Decision | Substantially Equivalent, Apr 7, 2015 |
| Received | Mar 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150580
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.