510(k) K860584 ยท KRG Programmer, Pacemaker
SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jun 6, 1986 |
| Received | Feb 18, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860584
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.