510(k) K092922 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
SSI-8000/S8/S6 DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM, 2P1 PHASED ARRAY DIAGNOSTIC ULTRASOUND TRANSDUCER
| Applicant | Sonoscape Company Limited, Dublin CA, US |
| Decision | Substantially Equivalent, Mar 12, 2010 |
| Received | Sep 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092922
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.