510(k) K792602 ยท DTC Analyzer, Pacemaker Generator Function
SUSI II PACEMAKER SURVEILLANCE MONITOR
| Applicant | Ela Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 25, 1980 |
| Received | Dec 18, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792602
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.