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Howtek, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021949FULCRUMAugust 12, 2002
K973081DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0)November 5, 1997
K972191DIGITIZER DIRECTOR (HSC025-01)September 8, 1997
K970908HOWTEK 960May 20, 1997
K953117SCANMASTER DXJanuary 18, 1996