510(k) K883602 ยท DTB Permanent Pacemaker Electrode
BIOPORE VS.1 ENDOCARDIAL INTER IMPLANT PACING LEAD
| Applicant | Intermedics, Inc., Freeport TX, US |
| Decision | Substantially Equivalent, Sep 6, 1988 |
| Received | Aug 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883602
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.