510(k) K133034 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
LOGIQ F SERIES
| Applicant | GE Healthcare, Wauwatosa WI, US |
| Decision | Substantially Equivalent, Jan 31, 2014 |
| Received | Sep 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133034
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.