510(k) K864629 ยท LBW Set, Dialysis, Single Needle (Co-Axial Flow)
MODIFIED DUAL LUMEN NEEDLE
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 16, 1986 |
| Received | Nov 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864629
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.