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Cefaly Acute

Page Type
Cleared 510(K)
510(k) Number
K171446
510(k) Type
Traditional
Applicant
CEFALY Technology
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
122 days
Submission Type
Summary

Cefaly Acute

Page Type
Cleared 510(K)
510(k) Number
K171446
510(k) Type
Traditional
Applicant
CEFALY Technology
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
122 days
Submission Type
Summary