510(k) K173923 ยท LDF Electrode, Pacemaker, Temporary
Temporary Cardiac Pacing Wire
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Aug 2, 2018 |
| Received | Dec 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173923
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.