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FibroScan® Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630)

Page Type
Cleared 510(K)
510(k) Number
K203273
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/25/2021
Days to Decision
139 days
Submission Type
Summary

FibroScan® Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630)

Page Type
Cleared 510(K)
510(k) Number
K203273
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/25/2021
Days to Decision
139 days
Submission Type
Summary