510(k) K904433 ยท LBW Set, Dialysis, Single Needle (Co-Axial Flow)
DUAL LUMEN NEEDLES
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Nov 23, 1990 |
| Received | Sep 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904433
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.