510(k) K880326 ยท DXY Implantable Pacemaker Pulse-Generator
MAESTRO(R) MODELS 115, 118, 215 AND 218 PACEMAKERS
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, Apr 11, 1988 |
| Received | Jan 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880326
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.