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VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K112213
510(k) Type
Traditional
Applicant
GE HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2011
Days to Decision
30 days
Submission Type
Summary

VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K112213
510(k) Type
Traditional
Applicant
GE HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2011
Days to Decision
30 days
Submission Type
Summary