K012452 is an FDA 510(k) clearance for the MODEL 6500 UNIPOLAR TEMORARY MYOCARDIAL PACING LEAD. This device is classified as a Electrode, Pacemaker, Temporary (Class II - Special Controls, product code LDF).
Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on August 14, 2001, 13 days after receiving the submission on August 1, 2001.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.3680.
| 510(k) Number | K012452 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 01, 2001 |
| Decision Date | August 14, 2001 |
| Days to Decision | 13 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | LDF — Electrode, Pacemaker, Temporary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.3680 |