510(k) K250381 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
Deepsight NeedleVue LC1 Ultrasound System
| Applicant | DeepSight Technology, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 1, 2025 |
| Received | Feb 11, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250381
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.