510(k) K092291 ยท DRX Electrode, Electrocardiograph
SKINTACT AND VARIOUS OTHER TRADENAMES
| Applicant | Leonhard Lang GmbH, Stillwater MN, US |
| Decision | Substantially Equivalent, Aug 21, 2009 |
| Received | Jul 29, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092291
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.