510(k) K963787 ยท DRX Electrode, Electrocardiograph
EXACTRACE ADULT FOAM MONITORING ECG ELECTRODE CONMED MODEL 1510 AND INSTATRACE ADULT DIAPHORETIC FOAM ECG ELECTRODE CONM
| Applicant | Conmedcorp, Utica NY, US |
| Decision | Substantially Equivalent, Mar 11, 1997 |
| Received | Sep 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963787
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.