510(k) K883743 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 4058 PACING LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 17, 1989 |
| Received | Sep 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883743
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 5, 2015 | Medtronic Inc. Cardiac Rhythm Disease Management Medtronic Medical Device Identification Card for SureScan pacemaker patients. The front of this card identifies the implanted pacing system components currently registered to the patient. Th Terminated |
DTB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.