510(k) K855000 ยท LDR Controller, Infusion, Intravascular, Electronic
RATEMINDER III INFUSION DEVICE
| Applicant | American Edwards Laboratories, Santa Ana CA, US |
| Decision | Substantially Equivalent, Feb 12, 1986 |
| Received | Dec 13, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855000
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.