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FibroScan 230

Page Type
Cleared 510(K)
510(k) Number
K212035
510(k) Type
Special
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/30/2021
Days to Decision
30 days
Submission Type
Summary

FibroScan 230

Page Type
Cleared 510(K)
510(k) Number
K212035
510(k) Type
Special
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/30/2021
Days to Decision
30 days
Submission Type
Summary