510(k) K780569 ยท DTB Permanent Pacemaker Electrode
L-12, L-21, AND L-22 ELECTRODES
| Applicant | Coratomic, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 14, 1978 |
| Received | Apr 11, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780569
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.