510(k) K950210 ยท DXY Implantable Pacemaker Pulse-Generator
CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., May 3, 1995 |
| Received | Jan 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950210
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.