510(k) K780908 ยท DRX Electrode, Electrocardiograph
SELF-RETAINING ELECTRODE SER. #4000-100
| Applicant | Andover Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 19, 1978 |
| Received | Jun 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780908
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.