510(k) K042369 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
SONOSCAPE ULTRASOUND SYSTEM SSI-1000/SSI-5000
| Applicant | Sonoscape Company Limited, Dublin CA, US |
| Decision | Substantially Equivalent, Oct 20, 2004 |
| Received | Aug 31, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042369
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.