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TE7/TE5/TE7 Max/TE5 Max/TE9 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K203391
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/23/2021
Days to Decision
125 days
Submission Type
Summary

TE7/TE5/TE7 Max/TE5 Max/TE9 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K203391
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/23/2021
Days to Decision
125 days
Submission Type
Summary