510(k) K882452 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODELS 4057/4557 ENDOCARDIAL PACING LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 25, 1988 |
| Received | Jun 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882452
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.