510(k) K920601 ยท DXY Implantable Pacemaker Pulse-Generator
ASTRA T2, ASTRA T4, ASTRA T6
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Oct 28, 1992 |
| Received | Feb 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920601
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.