510(k) K894679 ยท DRX Electrode, Electrocardiograph
ELECTROTRACE DISP. RESTING EKG ELECTRODES
| Applicant | Jason Marketing Co., Huntington Beach CA, US |
| Decision | Substantially Equivalent, Sep 13, 1989 |
| Received | Jul 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894679
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.