Te ME NA Sas
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) | K080603 | HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED | BSP | 2008-08-05 | View |
| 510(k) | K060186 | POLYPLEX STIMULATING CATHETER SYSTEM | CAZ | 2006-07-18 | View |
No matching devices.
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