510(k) K011457 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ALOKA SSD-5500 WITH KI AND A-SMA
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, May 23, 2001 |
| Received | May 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011457
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.