510(k) K890201 ยท DRX Electrode, Electrocardiograph
RADIOLUCENT ECG ELECTRODE MODEL NO: 1680
| Applicant | Medtronic Vascular, Haverhill MA, US |
| Decision | Substantially Equivalent, Mar 15, 1989 |
| Received | Jan 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890201
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.