510(k) K980423 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
SONOPSY LA SYSTEM
| Applicant | Neovision Corp., Norwalk CT, US |
| Decision | Substantially Equivalent, Aug 7, 1998 |
| Received | Feb 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980423
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.