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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181547
510(k) Type
Special
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/9/2018
Days to Decision
27 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181547
510(k) Type
Special
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/9/2018
Days to Decision
27 days
Submission Type
Summary