510(k) K032875 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM
| Applicant | Aloka Co. Ltd USA, Wallingford CT, US |
| Decision | Substantially Equivalent, Sep 30, 2003 |
| Received | Sep 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032875
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.