510(k) K170761 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
LIGHTSonic BUBM
| Applicant | Lightmed USA, Inc., San Clemente CA, US |
| Decision | Substantially Equivalent, Apr 13, 2018 |
| Received | Mar 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170761
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.