510(k) K873772 ยท DTB Permanent Pacemaker Electrode
CHANGES TO ENCOR PERVENOUS J-ATRIAL LEADS
| Applicant | Cordis Leads, Inc., Suffield CT, US |
| Decision | Substantially Equivalent, Oct 19, 1988 |
| Received | Sep 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873772
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.