FDA 510(k) Applications Submitted by HOWTEK, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K021949 | 06/13/2002 | FULCRUM | HOWTEK, INC. |
| K970908 | 03/11/1997 | HOWTEK 960 | HOWTEK, INC. |
| K953117 | 07/03/1995 | SCANMASTER DX | HOWTEK, INC. |
| 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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