510(k) K944655 ยท DRX Electrode, Electrocardiograph
ECG ELECTRODE
| Applicant | Conmed Andover Medical, Inc., Haverhill MA, US |
| Decision | Substantially Equivalent, Nov 22, 1994 |
| Received | Sep 21, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944655
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.