510(k) K890103 ยท DRX Electrode, Electrocardiograph
BARD TAB ECG MONITORING ELECTRODE
| Applicant | C.R. Bard, Inc., Tewksbury MA, US |
| Decision | Substantially Equivalent, Jan 24, 1989 |
| Received | Jan 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890103
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.