510(k) K910237 ยท DTE Pulse-Generator, Pacemaker, External
MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 25, 1991 |
| Received | Jan 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910237
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.