Medi-Dyne, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K000825 | 4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER | DQO | 2000-09-21 | View |
| 510(k) | K970401 | MEDI-DYNE GUIDING CATHETER | DQY | 1997-08-01 | View |
| 510(k) | K931833 | MODIFIED LUER | DQO | 1993-09-28 | View |
| 510(k) | K930694 | MEDI-DYNE ANGIOGRAPHIC CATHETER | DQO | 1993-08-02 | View |
No matching devices.
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