510(k) K792301 ยท DTB Permanent Pacemaker Electrode
LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL
| Applicant | Intermedics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 4, 1980 |
| Received | Nov 15, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792301
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.