510(k) K820179 ยท FKX System, Peritoneal, Automatic Delivery
ERIKA CAPD PREP KIT #30-9501-5
| Applicant | Erika, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 19, 1982 |
| Received | Jan 22, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820179
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.