510(k) K910173 ยท FKX System, Peritoneal, Automatic Delivery
SELECTRA AND TUBING SETS
| Applicant | Medionics International , Ltd., Canada L6e 1a5, CA |
| Decision | Substantially Equivalent, Jan 13, 1992 |
| Received | Jan 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910173
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.