510(k) K925430 ยท FPA Set, Administration, Intravascular
LO-PROFILE EXTENSIONSET W/ .22 MICRON FILTER
| Applicant | Douglas Medical Products Corp., Mundelein IL, US |
| Decision | Substantially Equivalent, Aug 3, 1993 |
| Received | Oct 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925430
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.