510(k) K760280 ยท DRX Electrode, Electrocardiograph
ELECTRODE SERIES 1401
| Applicant | Andover Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 23, 1976 |
| Received | Jul 23, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760280
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.