510(k) K893425 ยท DRX Electrode, Electrocardiograph
VITATRACE
| Applicant | Lectec Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jul 14, 1989 |
| Received | May 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893425
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.