Last synced on 20 December 2024 at 11:05 pm

SKR 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182688
510(k) Type
Special
Applicant
KONICA MINOLTA, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/18/2018
Days to Decision
83 days
Submission Type
Summary

SKR 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182688
510(k) Type
Special
Applicant
KONICA MINOLTA, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
12/18/2018
Days to Decision
83 days
Submission Type
Summary