FDA 510(k) Applications Submitted by BRAINBASE CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K052254 | 08/18/2005 | MYTIS ARROW XXXX | BRAINBASE CORPORATION |
| K083372 | 11/14/2008 | ARROWBONE-A, ARROWBONE-B | BRAINBASE CORPORATION |
| K063236 | 10/25/2006 | BETA-POWDER | BRAINBASE CORPORATION |
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