510(k) K961833 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
SONOLINE ELEGRA WITH SIESCAPE FEATURE
| Applicant | Siemens Medical Solutions USA, Inc., Issaquah WA, US |
| Decision | Substantially Equivalent, Oct 29, 1996 |
| Received | May 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961833
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.