Last synced on 14 November 2025 at 11:06 pm

Voluson™ Performance 16; Voluson™ Performance 18

Page Type
Cleared 510(K)
510(k) Number
K250543
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2025
Days to Decision
94 days
Submission Type
Summary

Voluson™ Performance 16; Voluson™ Performance 18

Page Type
Cleared 510(K)
510(k) Number
K250543
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2025
Days to Decision
94 days
Submission Type
Summary