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Ultrasound System SONIMAGE MX1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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