510(k) K970901 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Dec 22, 1997 |
| Received | Mar 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970901
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.