510(k) K953417 ยท DXY Implantable Pacemaker Pulse-Generator
MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS
| Applicant | Cook Pacemaker Corp., Leechburg PA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Sep 29, 1995 |
| Received | Jun 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953417
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.