510(k) K895495 ยท DXY Implantable Pacemaker Pulse-Generator
ADD'L LABELING TO MINIX MODELS AND MINIX ST MODELS
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Aug 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895495
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.