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DIRECT DIGITIZER, REGIUS MODEL 190

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042386
510(k) Type
Special
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/15/2004
Days to Decision
104 days
Submission Type
Summary

DIRECT DIGITIZER, REGIUS MODEL 190

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042386
510(k) Type
Special
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/15/2004
Days to Decision
104 days
Submission Type
Summary