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UltraVision 2 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K173265
510(k) Type
Abbreviated
Applicant
WinProbe Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
27 days
Submission Type
Summary

UltraVision 2 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K173265
510(k) Type
Abbreviated
Applicant
WinProbe Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
27 days
Submission Type
Summary