ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE — Microvena Corp. (510(k) K991898)
ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE — Microvena Corp. (510(k) K991898) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE; Applicant: Microvena Corp.; Clearance track: 510(k).
| Device name | ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE |
|---|---|
| Applicant | Microvena Corp. |
| Clearance track | 510(k) |
| Submission number | K991898 |
| Decision | Substantially Equivalent |
| Decision date | 1999-06-16 |
| Date received | 1999-06-04 |
| Product code | DQX |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | MN, US |
| Source | openFDA device |
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$1999/mo
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