510(k) K900805 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ALOKA 500 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM
| Applicant | Ge Medical Systems Information Technologies, Wallingford CT, US |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | Feb 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900805
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.