Last synced on 25 April 2025 at 11:05 pm

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213642
510(k) Type
Traditional
Applicant
GE Healthcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2022
Days to Decision
56 days
Submission Type
Summary

Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213642
510(k) Type
Traditional
Applicant
GE Healthcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2022
Days to Decision
56 days
Submission Type
Summary