Activiews, Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120300 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | JAK | 2012-04-13 | View |
| 510(k) | K113063 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | JAK | 2011-11-10 | View |
| 510(k) | K110812 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | JAK | 2011-06-21 | View |
No matching devices.
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