510(k) K890288 ยท FJS Catheter, Peritoneal, Long-Term Indwelling
PERITONEAL CATHETERS WITH AN ADDED FUNCTION
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Mar 27, 1989 |
| Received | Jan 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890288
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.