510(k) K923868 ยท DXY Implantable Pacemaker Pulse-Generator
CCS MAESTRO II SERIES 200 CARDIAC PACEMAKER
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, May 14, 1993 |
| Received | Aug 3, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923868
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.