510(k) K024264 ยท DRX Electrode, Electrocardiograph
SKINTACT
| Applicant | Leonhard Lang Co., Stillwater MN, US |
| Decision | Substantially Equivalent, Jan 16, 2003 |
| Received | Dec 23, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K024264
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.