510(k) K951449 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
MODEL KM-25
| Applicant | Koven Technology, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, May 20, 1996 |
| Received | Mar 29, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951449
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.