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FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223902
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/2/2023
Days to Decision
64 days
Submission Type
Summary

FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223902
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/2/2023
Days to Decision
64 days
Submission Type
Summary