510(k) K062760 ยท DRX Electrode, Electrocardiograph
ORI F6T DRY ECG MONITORING ELECTRODE
| Applicant | Orbital Research, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 11, 2006 |
| Received | Sep 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062760
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.