510(k) K960700 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 28, 1996 |
| Received | Feb 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960700
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.