K050873 is an FDA 510(k) clearance for the CANALIZER HYDROPHILIC GUIDE WIRE. This device is classified as a Wire, Guide, Catheter (Class II - Special Controls, product code DQX).
Submitted by Medical Device Technologies, Inc. (Gainesville, US). The FDA issued a Cleared decision on May 26, 2005, 50 days after receiving the submission on April 6, 2005.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1330.
| 510(k) Number | K050873 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 06, 2005 |
| Decision Date | May 26, 2005 |
| Days to Decision | 50 days |
| Submission Type | Traditional |
| 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 |