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

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