510(k) K760013 ยท DTC Analyzer, Pacemaker Generator Function
PACER SYSTEMS ANALYZER (CORDIS)
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1976 |
| Received | Jun 10, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760013
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.