510(k) K023920 ยท DRX Electrode, Electrocardiograph
SKINTACT
| Applicant | Leonhard Lang GmbH, Stillwater MN, US |
| Decision | Substantially Equivalent, Jan 16, 2003 |
| Received | Nov 25, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023920
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.