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KONICA DIRECT DIGITIZER REGIUS, MODEL 170

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023061
510(k) Type
Special
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
25 days
Submission Type
Statement

KONICA DIRECT DIGITIZER REGIUS, MODEL 170

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023061
510(k) Type
Special
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/11/2002
Days to Decision
25 days
Submission Type
Statement