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U-Lite EXP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171164
510(k) Type
Traditional
Applicant
Sonoscanner
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/3/2017
Days to Decision
105 days
Submission Type
Summary

U-Lite EXP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171164
510(k) Type
Traditional
Applicant
Sonoscanner
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/3/2017
Days to Decision
105 days
Submission Type
Summary