510(k) K803042 ยท DTB Permanent Pacemaker Electrode
SIEMENS-ELEMA ENDOCARDIAL LEAD 402S
| Applicant | Siemens Elema AB, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 22, 1980 |
| Received | Dec 1, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803042
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.