Compression Works, LLC
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) | K133029 | ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE | DXC | 2013-12-06 | View |
| 510(k) | K112384 | ABDOMINAL TOURNIQUET SYSTEM | DXC | 2011-10-18 | View |
No matching devices.
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