510(k) K040719 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ALOKA MODEL SSD-4000 DIAGNOSTIC ULTRASOUND SYSTEM W/OPTIONAL SONOREAL 3D SYSTEM ACCESSORY
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Mar 26, 2004 |
| Received | Mar 19, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040719
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.