510(k) K880422 ยท DXY Implantable Pacemaker Pulse-Generator
MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, Mar 31, 1988 |
| Received | Feb 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880422
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.