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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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