510(k) K942441 ยท JAF Monitor, Ultrasonic, Nonfetal
IMEXDOP CT+
| Applicant | Imex Medical Systems, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Aug 23, 1994 |
| Received | May 23, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942441
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.