510(k) K885262 ยท DRX Electrode, Electrocardiograph
POLYHESIVE MONITORING AND DIAGNOSTIC ELECTRODES
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Jan 25, 1989 |
| Received | Dec 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885262
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.