Guidewire Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K902153 | TEFLON COATED GUIDEWIRE | DQX | 1990-07-31 | View |
| 510(k) | K902152 | MOVABLE CORE GUIDEWIRE | DQX | 1990-07-31 | View |
| 510(k) | K890959 | GUIDEWIRE | DQX | 1989-09-12 | View |
No matching devices.
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