510(k) K003739 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ALOKA SSD-4000
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Dec 27, 2000 |
| Received | Dec 4, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K003739
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.