510(k) K885240 ยท DTB Permanent Pacemaker Electrode
MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD
| Applicant | Tpl-Cordis, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Feb 10, 1989 |
| Received | Dec 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885240
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.