510(k) K865013 ยท DXY Implantable Pacemaker Pulse-Generator
ASTRA T2, T4 AND T6
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Feb 19, 1987 |
| Received | Dec 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K865013
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.