FDA 510(k) Applications Submitted by RUSSELL LEONARD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972191 | 06/10/1997 | DIGITIZER DIRECTOR (HSC025-01) | HOWTEK, INC. |
| K973081 | 08/18/1997 | DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0) | HOWTEK, INC. |
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