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AUTOMATED BREAST ULTRASOUND SYSTEM, MODEL ABUS

Page Type
Cleared 510(K)
510(k) Number
K052355
510(k) Type
Special
Applicant
U-SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2005
Days to Decision
16 days
Submission Type
Summary

AUTOMATED BREAST ULTRASOUND SYSTEM, MODEL ABUS

Page Type
Cleared 510(K)
510(k) Number
K052355
510(k) Type
Special
Applicant
U-SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2005
Days to Decision
16 days
Submission Type
Summary