510(k) K873442 ยท DRX Electrode, Electrocardiograph
ECG ELECTRODE SYSTEM
| Applicant | Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S, Cambridge MA, US |
| Decision | Substantially Equivalent, Nov 23, 1987 |
| Received | Aug 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873442
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.