510(k) K791140 ยท DRX Electrode, Electrocardiograph
PREGELLED DISPOSABLE EELCTRO. SERIES 600
| Applicant | Hayes Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 10, 1979 |
| Received | Jun 18, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791140
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.