510(k) K173265 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
UltraVision 2 Diagnostic Ultrasound System
| Applicant | Winprobe Corporation, Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Nov 7, 2017 |
| Received | Oct 11, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K173265
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.