510(k) K844630 ยท FKX System, Peritoneal, Automatic Delivery
ROPE SYSTEM REVERSE OSMOSIS PERITONEAL SYSTEM
| Applicant | Organon Teknika Corp., Oklahoma City OK, US |
| Decision | Substantially Equivalent, Mar 12, 1985 |
| Received | Nov 27, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844630
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.