510(k) K182529 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Xperius Ultrasound System
| Applicant | Philips Ultrasound, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Oct 23, 2018 |
| Received | Sep 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182529
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.