510(k) K862655 ยท DRX Electrode, Electrocardiograph
SIGNA II RESTING ECG ELECTRODE
| Applicant | Kone Instruments, Inc., Milton WI, US |
| Decision | Substantially Equivalent, Aug 6, 1986 |
| Received | Jul 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862655
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.