510(k) K781456 ยท DTB Permanent Pacemaker Electrode
ENDOCARDIAL BIPOLAR LEAD
| Applicant | American Technology, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 4, 1978 |
| Received | Aug 23, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781456
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.