510(k) K020382 ยท DRX Electrode, Electrocardiograph
BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA
| Applicant | Medicotest A/S, Washington DC, US |
| Decision | Substantially Equivalent, Jun 28, 2002 |
| Received | Feb 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020382
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.