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Konicaminolta DI-X1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230906
510(k) Type
Special
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/25/2023
Days to Decision
25 days
Submission Type
Summary

Konicaminolta DI-X1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230906
510(k) Type
Special
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/25/2023
Days to Decision
25 days
Submission Type
Summary