510(k) K862038 ยท DXY Implantable Pacemaker Pulse-Generator
MODIFY LABEL/SPECTRAX S & SX IMPLANT PULSE GENER
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 17, 1986 |
| Received | May 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862038
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.