510(k) K830881 ยท FKX System, Peritoneal, Automatic Delivery
AMPERCIDE DISINFECTANT ACCESSORY TO -
| Applicant | American Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 2, 1983 |
| Received | Mar 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830881
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.