510(k) K183173 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
LIGHTMED Ultrasound System
| Applicant | Lightmed USA, Inc., San Clemente CA, US |
| Decision | Substantially Equivalent, Jul 1, 2019 |
| Received | Nov 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183173
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.