510(k) K803313 ยท DTE Pulse-Generator, Pacemaker, External
PACING SYSTEM ANALYZER
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Feb 23, 1981 |
| Received | Dec 31, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803313
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.