510(k) K950751 ยท DXY Implantable Pacemaker Pulse-Generator
TECOTHANE 75D POLYURETHANE RESIN FOR PULSE GENERATOR CONNECTOR MODULES
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., May 15, 1995 |
| Received | Feb 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950751
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.