510(k) K161224 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3
| Applicant | GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC, Wauwatosa WI, US |
| Decision | Substantially Equivalent, Aug 5, 2016 |
| Received | Apr 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161224
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.