510(k) K834106 ยท LDR Controller, Infusion, Intravascular, Electronic
INTRAVENOUS INFUSION CONTROLLER
| Applicant | Cutter Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 30, 1984 |
| Received | Nov 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834106
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.