510(k) K854433 ยท DRX Electrode, Electrocardiograph
ECG MONITORING/DEFIBRILLATION ELECTRODE
| Applicant | Andover Medical, Inc., Lawrence MA, US |
| Decision | Substantially Equivalent, May 8, 1986 |
| Received | Nov 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854433
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.