510(k) K932254 ยท DTB Permanent Pacemaker Electrode
MAXIMA FILTERED HARDSHELL RESERVOIR
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Unknown, Aug 3, 1993 |
| Received | May 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932254
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.