CORDIS HYDRONOL STEERABLE GUIDEWIRE — Cordis Corp. (510(k) K973845)
CORDIS HYDRONOL STEERABLE GUIDEWIRE — Cordis Corp. (510(k) K973845) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: CORDIS HYDRONOL STEERABLE GUIDEWIRE; Applicant: Cordis Corp.; Clearance track: 510(k).
| Device name | CORDIS HYDRONOL STEERABLE GUIDEWIRE |
|---|---|
| Applicant | Cordis Corp. |
| Clearance track | 510(k) |
| Submission number | K973845 |
| Decision | Substantially Equivalent |
| Decision date | 1998-01-05 |
| Date received | 1997-10-08 |
| Product code | DQX |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | FL, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →