Brainbase Corporation
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) | K083372 | ARROWBONE-A, ARROWBONE-B | LYC | 2009-12-08 | View |
| 510(k) | K063236 | BETA-POWDER | KOJ | 2007-02-16 | View |
| 510(k) | K052254 | MYTIS ARROW XXXX | DZE | 2006-06-01 | View |
No matching devices.
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