510(k) K905824 ยท DXY Implantable Pacemaker Pulse-Generator
MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, May 16, 1991 |
| Received | Dec 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905824
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.