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SKR 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171716
510(k) Type
Traditional
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/25/2017
Days to Decision
77 days
Submission Type
Statement

SKR 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171716
510(k) Type
Traditional
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/25/2017
Days to Decision
77 days
Submission Type
Statement