Last synced on 12 July 2024 at 11:04 pm

DRY LASER IMAGER, DRYPRO MODEL 832

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061999
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/15/2006
Days to Decision
32 days
Submission Type
Summary

DRY LASER IMAGER, DRYPRO MODEL 832

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061999
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/15/2006
Days to Decision
32 days
Submission Type
Summary