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Cefaly Dual

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173006
510(k) Type
Traditional
Applicant
CEFALY Technology
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
11/28/2017
Days to Decision
62 days
Submission Type
Summary

Cefaly Dual

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173006
510(k) Type
Traditional
Applicant
CEFALY Technology
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
11/28/2017
Days to Decision
62 days
Submission Type
Summary