Alure Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K092538 | REFINE SUPPORT SYSTEM, MODEL 100.0100 | FTL | 2010-03-05 | View |
| 510(k) | K083102 | REFINE LIFT SYSTEM | FTL | 2009-05-11 | View |
No matching devices.
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