510(k) K161249 ยท LDF Electrode, Pacemaker, Temporary
Streamline 6495 Bipolar Temporary Myocardial Pacing Lead
| Applicant | Medtronic, Santa Ana CA, US |
| Decision | Substantially Equivalent, Aug 19, 2016 |
| Received | May 3, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161249
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.