510(k) K884023 ยท DXY Implantable Pacemaker Pulse-Generator
MAESTRO(R) SERIES 100/200 SINGLE CHAMBER PACEMAKER
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, Oct 17, 1988 |
| Received | Sep 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884023
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.