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Biim Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K173138
510(k) Type
Traditional
Applicant
Biim Ultrasound AS
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
10/27/2017
Days to Decision
28 days
Submission Type
Summary

Biim Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K173138
510(k) Type
Traditional
Applicant
Biim Ultrasound AS
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
10/27/2017
Days to Decision
28 days
Submission Type
Summary