Last synced on 19 July 2024 at 11:05 pm

MODIFICATION TO: 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
K052095
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
11/3/2005
Days to Decision
101 days
Submission Type
Summary

MODIFICATION TO: 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
K052095
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
11/3/2005
Days to Decision
101 days
Submission Type
Summary