Medtronic · Class II · Cleared May 25, 2017
| K-number | K171253 |
| Device name | 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 |
| Product code | LDF |
| Device class | Class II |
| Decision date | May 25, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 870.3680 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov