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Biim Diagnostic Ultrasound System

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