510(k) K161873 ยท LDF Electrode, Pacemaker, Temporary
Pacel Flow Directed Pacing Catheter
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Nov 22, 2016 |
| Received | Jul 7, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161873
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.