510(k) K941652 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ALOKA SSD-2000 DIAGNOSTIC ULTRASOUND SYSTEM MODIFICATION
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Oct 21, 1994 |
| Received | Apr 5, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941652
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.