510(k) K850652 ยท DTD Pacemaker Lead Adaptor
PACESETTER SYSTEMS, ENDOCARDIAL FIRM LEAD
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Apr 10, 1985 |
| Received | Feb 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850652
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.