510(k) K883203 ยท DTB Permanent Pacemaker Electrode
MODEL 5866-34A PACEMAKER LEAD ADAPTOR
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 6, 1988 |
| Received | Jul 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883203
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.