Aurora Imaging Technology, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K073425 | MODIFICATION TO AURORA MRI SYSTEM | LNH | 2008-09-16 | View |
| 510(k) | K052698 | MODIFICATION TO: AURORA | LNH | 2005-11-08 | View |
| 510(k) | K032678 | MODIFICATION TO: AURORA | LNH | 2003-09-24 | View |
| 510(k) | K032082 | AURORA | LNH | 2003-07-30 | View |
| 510(k) | K023686 | AURORA MR-GUIDED INTERVENTIONAL SYSTEM | LNH | 2003-01-29 | View |
| 510(k) | K012154 | AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE | LNH | 2001-09-19 | View |
| 510(k) | K003651 | AURORA | LNH | 2001-02-21 | View |
No matching devices.
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