510(k) K883755 ยท DXY Implantable Pacemaker Pulse-Generator
MODIFIED SPECTRAX SX/SXT & PASYS/PASYS ST MODELS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 17, 1988 |
| Received | Sep 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883755
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.