510(k) K881749 ยท GXY Electrode, Cutaneous
STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | Apr 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881749
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.