510(k) K890785 ยท DXY Implantable Pacemaker Pulse-Generator
ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Mar 10, 1989 |
| Received | Feb 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890785
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.