510(k) K153760 ยท LDR Controller, Infusion, Intravascular, Electronic
Volumetric Infusion Controller
| Applicant | DEKA Research & Development, Manchester NH, US |
| Decision | Substantially Equivalent, Oct 3, 2016 |
| Received | Dec 30, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153760
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.