510(k) K905029 ยท FRN Pump, Infusion
MODEL 2001, MODIFICATION
| Applicant | Medfusion, Inc., Duluth GA, US |
| Decision | Substantially Equivalent, Dec 24, 1990 |
| Received | Oct 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905029
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.