K083713 is an FDA 510(k) clearance for the .035 LOC GUIDE WIRE EXTENSION. This device is classified as a Wire, Guide, Catheter (Class II - Special Controls, product code DQX).
Submitted by Abbott Vascular (Santa Clara, US). The FDA issued a Cleared decision on February 23, 2009, 70 days after receiving the submission on December 15, 2008.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1330.
| 510(k) Number | K083713 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 15, 2008 |
| Decision Date | February 23, 2009 |
| Days to Decision | 70 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DQX — Wire, Guide, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1330 |