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Bone Suppression Software

Page Type
Cleared 510(K)
510(k) Number
K240281
510(k) Type
Traditional
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/31/2024
Days to Decision
120 days
Submission Type
Summary

Bone Suppression Software

Page Type
Cleared 510(K)
510(k) Number
K240281
510(k) Type
Traditional
Applicant
Konica Minolta, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/31/2024
Days to Decision
120 days
Submission Type
Summary