510(k) K893633 ยท DTE Pulse-Generator, Pacemaker, External
MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | May 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893633
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.