510(k) K102642 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
SONOSCAPE ULTRASOUND SYSTEM AND TRANSDUCERS MODEL SSI-8000, 2P1 PHASED ARRAY, 5P1 PHASED ARRAY MODEL 2P1, 5P1, 6V1 MICRO
| Applicant | Sonoscape Company Limited, Hayward CA, US |
| Decision | Substantially Equivalent, Mar 4, 2011 |
| Received | Sep 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102642
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.