510(k) K171253 ยท LDF Electrode, Pacemaker, Temporary
Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Pacing Lead, Streamline 6495 Bipolar Temporary Myocardial Pacing Lead, Streamline 6500 Unipolar Temporary Myocardial Pacing Lead
| Applicant | Medtronic, Santa Ana CA, US |
| Decision | Substantially Equivalent, May 25, 2017 |
| Received | Apr 28, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171253
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.