510(k) K961040 ยท FJI Dialyzer, Capillary, Hollow Fiber
BLOOD PORT CAP, DIALYSATE PORT CAP, RED HARD PLASTIC
| Applicant | Dayspring Medical, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Jun 11, 1996 |
| Received | Mar 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961040
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.