510(k) K923558 ยท DRX Electrode, Electrocardiograph
ECG ELECTRODE
| Applicant | Lectec Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Feb 18, 1993 |
| Received | Jul 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923558
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.