510(k) K790503 ยท DTA Tester, Pacemaker Electrode Function
CARDIOTEST 2200
| Applicant | Cardiac Pacemakers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 17, 1979 |
| Received | Mar 13, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790503
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.