510(k) K951087 ยท DTB Permanent Pacemaker Electrode
TENDRIL, UNIPOLAR ENDOCARDIAL SCREW-IN LEAD
| Applicant | Pacesetter, Inc., Sylmar CA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 29, 1995 |
| Received | Mar 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951087
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.