510(k) K823896 ยท DTB Permanent Pacemaker Electrode
MODEL FF..D & FX..D PACEMAKER LEADS
| Applicant | Dr. Ing. P. Osypka, GmbH, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 30, 1983 |
| Received | Dec 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823896
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.