510(k) K930854 ยท FPA Set, Administration, Intravascular
SOLUTION SET WITH .2 MICRON FILTER
| Applicant | Douglas Medical Products Corp., Mundelein IL, US |
| Decision | Substantially Equivalent, Jan 14, 1994 |
| Received | Feb 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930854
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.