510(k) K840439 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
RECOMED CARDIAC OUTPUT METER 236067-
| Applicant | Litton Medical Electronics, Elk Grove Village IL, US |
| Decision | Substantially Equivalent, Nov 20, 1984 |
| Received | Feb 1, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840439
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.