510(k) K954022 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ALOKA OMNIVIEW DIAGNOSTIC ULTRASOUND SYSTEM
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Jan 17, 1996 |
| Received | Aug 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954022
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.