510(k) K910494 ยท DRX Electrode, Electrocardiograph
RESTING EKG ELECTRODE SERIES
| Applicant | Medtronic Andover Medical, Inc., Haverhill MA, US |
| Decision | Substantially Equivalent, Apr 22, 1991 |
| Received | Feb 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910494
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.