510(k) K904512 ยท DRX Electrode, Electrocardiograph
TRACET AG 4000
| Applicant | Lectec Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jan 31, 1991 |
| Received | Oct 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904512
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.