510(k) K781940 ยท DRX Electrode, Electrocardiograph
EKG ELECTRODES, DISPOSABLE
| Applicant | Hayes Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 29, 1978 |
| Received | Nov 20, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781940
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.