510(k) K933069 ยท DTA Tester, Pacemaker Electrode Function
MODEL EP-2 CLINICAL STIMULATOR
| Applicant | Ep Medical, Inc., Budd Lake NJ, US |
| Decision | Substantially Equivalent, Oct 21, 1993 |
| Received | Jun 22, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933069
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.