FDA 510(k) Applications Submitted by TOM BONNER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110358 | 02/07/2011 | VENODYNE V810 | MICROTEK MEDICAL, INC. |
| K970547 | 02/12/1997 | ISOLYSER SDS SHARPS CONTAINER | THANTEX SPECIALTIES, INC. |
| K011318 | 05/01/2001 | VENODYNE DVT ADVANTAGE PLUS | MICROTEK MEDICAL, INC. |
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