510(k) K982123 ยท FPA Set, Administration, Intravascular
CONTRAST CONTROL DEVICE
| Applicant | Medex, Inc., Hilliard OH, US |
| Decision | Substantially Equivalent, Jul 21, 1998 |
| Received | Jun 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982123
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.