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Ultrasound System SONIMAGE MX1

Page Type
Cleared 510(K)
510(k) Number
K220993
510(k) Type
Traditional
Applicant
Konica Minolta, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/23/2022
Days to Decision
80 days
Submission Type
Summary

Ultrasound System SONIMAGE MX1

Page Type
Cleared 510(K)
510(k) Number
K220993
510(k) Type
Traditional
Applicant
Konica Minolta, INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/23/2022
Days to Decision
80 days
Submission Type
Summary