510(k) K870472 ยท FKO Catheter, Peritoneal Dialysis, Single Use
ACUTE PERITONEAL DIALYSIS KIT
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Feb 25, 1987 |
| Received | Feb 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870472
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.