510(k) K883855 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
PREDICTOR II SIGNAL AVERAGING ECG
| Applicant | Corazonix Corp., Oklahoma City OK, US |
| Decision | Substantially Equivalent, Nov 3, 1988 |
| Received | Sep 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883855
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.