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FDA 510(k) Applications Submitted by CEFALY TECHNOLOGY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160237
02/01/2016
Cefaly
CEFALY TECHNOLOGY
K171446
05/16/2017
Cefaly Acute
CEFALY Technology
K173006
09/27/2017
Cefaly Dual
CEFALY Technology
K201895
07/08/2020
Cefaly Dual
CEFALY Technology
K212071
07/02/2021
Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx, Cefaly Dual Connected - OTC, Cefaly Dual Connected - Rx
CEFALY Technology
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