510(k) K041916 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ALOKA SSD-ALPHA 5 ULTRASOUND SYSTEM
| Applicant | Aloka Co. Ltd USA, Wallingford CT, US |
| Decision | Substantially Equivalent, Jul 30, 2004 |
| Received | Jul 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041916
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.