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DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973081
510(k) Type
Traditional
Applicant
Howtek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
79 days
Submission Type
Summary

DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973081
510(k) Type
Traditional
Applicant
Howtek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
79 days
Submission Type
Summary