510(k) K862053 ยท DTB Permanent Pacemaker Electrode
MODEL 432-01 BIOPORE IMPLANTABLE PACING LEAD
| Applicant | Intermedics, Inc., Freeport TX, US |
| Decision | Substantially Equivalent, Sep 19, 1986 |
| Received | May 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862053
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.