510(k) K895136 ยท DTB Permanent Pacemaker Electrode
PERMANENT AND TEMP. PACEMAKER ELECTRODE & LEAD ADA
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 8, 1990 |
| Received | Aug 16, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895136
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.