510(k) K961936 ยท DTB Permanent Pacemaker Electrode
MODEL 2188 CORONARY SINUS LEAD.
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Aug 15, 1996 |
| Received | May 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961936
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.