510(k) K932172 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODELS 4057M,4058M,4557M, PACING LEADS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Unknown, Dec 8, 1993 |
| Received | May 5, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932172
| 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.