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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
K173034
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2017
Days to Decision
47 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
K173034
510(k) Type
Traditional
Applicant
Echosens
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2017
Days to Decision
47 days
Submission Type
Summary