510(k) K844748 ยท FKQ System, Dialysate Delivery, Central Multiple Patient
NEPHROSS ALLEGRO H.F.
| Applicant | Organon Teknika Corp., Oklahoma City OK, US |
| Decision | Substantially Equivalent, Jan 22, 1985 |
| Received | Dec 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844748
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.