510(k) K841739 ยท DTD Pacemaker Lead Adaptor
MODEL 866 PERMATHANE BIPOLAR, COAXIAL
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 3, 1984 |
| Received | Apr 27, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841739
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.