510(k) K900984 ยท DTB Permanent Pacemaker Electrode
MODIFIED UNIPOLAR IMPLANT. PACING LEADS W/IS-1
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 3, 1990 |
| Received | Mar 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900984
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.