510(k) K242693 ยท LDR Controller, Infusion, Intravascular, Electronic
DEKA Infusion System, DEKA Administration Set
| Applicant | Deka Research and Development Corporation, Manchester NH, US |
| Decision | Substantially Equivalent, Oct 7, 2024 |
| Received | Sep 9, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242693
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.