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Howtek, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K021949	FULCRUM	LMA	2002-08-12	View
510(k)	K973081	DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0)	LLZ	1997-11-05	View
510(k)	K972191	DIGITIZER DIRECTOR (HSC025-01)	LMD	1997-09-08	View
510(k)	K970908	HOWTEK 960	LMA	1997-05-20	View
510(k)	K953117	SCANMASTER DX	LMA	1996-01-18	View

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