510(k) K013950 ยท FPA Set, Administration, Intravascular
VENTED VIAL ACCESS DEVICE
| Applicant | Churchill Medical Systems, Inc., Dover NH, US |
| Decision | Substantially Equivalent, Jan 10, 2002 |
| Received | Nov 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013950
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.