510(k) K973727 ยท DRX Electrode, Electrocardiograph
ELECTRODE, ELECTROCARDIOGRAPH
| Applicant | Don Tay Industries, New Berlin WI, US |
| Decision | Substantially Equivalent, Dec 19, 1997 |
| Received | Sep 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973727
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.