510(k) K843141 ยท LDF Electrode, Pacemaker, Temporary
CRITIKON HEPARIN-COATED CARDIOVASCULAR
| Applicant | Critikon Company, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Sep 4, 1984 |
| Received | Aug 9, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843141
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.