510(k) K930964 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE)
| Applicant | Acuson Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, Oct 26, 1994 |
| Received | Feb 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930964
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.