510(k) K032926 ยท KRE Analyzer, Pacemaker Generator Function, Indirect
EKG SPEAKS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 15, 2003 |
| Received | Sep 22, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032926
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.