510(k) K904941 ยท DXY Implantable Pacemaker Pulse-Generator
MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE
| Applicant | Cardiac Control Systems, Inc., Palm Coast FL, US |
| Decision | Substantially Equivalent, Jan 3, 1991 |
| Received | Nov 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904941
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.