510(k) K842394 ยท DXY Implantable Pacemaker Pulse-Generator
ASTRA 2, ASTRA 3, 4 & 6
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Oct 17, 1984 |
| Received | Jun 19, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842394
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.