510(k) K863204 ยท LDR Controller, Infusion, Intravascular, Electronic
DEKA JR.
| Applicant | Deka Research & Development Corp., Manchester NH, US |
| Decision | Substantially Equivalent, Sep 3, 1986 |
| Received | Aug 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863204
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.