510(k) K862071 ยท DXY Implantable Pacemaker Pulse-Generator
MODIFIED LABEL FOR/SPECTRAX SXT IMPLANT. PULSE GEN
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 17, 1986 |
| Received | May 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862071
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.