510(k) K950473 ยท DRX Electrode, Electrocardiograph
DISPOSABLE ECG MONITORING ELECTRODE
| Applicant | Nikomed U.S.A., Inc., Doylestown PA, US |
| Decision | Substantially Equivalent, Dec 12, 1995 |
| Received | Feb 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950473
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.