Schneider (Europe) GmbH
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K984068 | FLAMINGO WALLSTENT ESOPHAGEAL ENDOPROSTHESIS | ESW | 1999-01-07 | View |
| 510(k) | K982592 | DOCKING-EXTENSION WIRE | DQX | 1998-10-21 | View |
| 510(k) | K970528 | CLYDE CORONARY GUIDEWIRE | DQX | 1997-06-10 | View |
| 510(k) | K970494 | HANNIBAL GUIDEWIRE | DQX | 1997-05-09 | View |
| 510(k) | K951109 | C-THRU CORONARY GUIDE WIRE | DQX | 1995-06-08 | View |
No matching devices.
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