510(k) K893909 ยท FPA Set, Administration, Intravascular
MODIFIED MATERIAL USED IN INFUSION T
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 25, 1989 |
| Received | May 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893909
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.