510(k) K896632 ยท DTC Analyzer, Pacemaker Generator Function
MEDTRONIC MODEL 5401B TEST CABLE
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 13, 1989 |
| Received | Nov 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896632
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.