510(k) K010950 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
CYPRESS SYSTEM
| Applicant | Acuson Corp., Washington DC, US |
| Decision | Substantially Equivalent, Jun 27, 2001 |
| Received | Mar 29, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K010950
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.