FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

Cefaly Dual

K Number: K201895 · Decision Sep 29, 2020
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
17
Applicant Total
6
Review Days
83

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Basic Information

Device Name
Cefaly Dual
K Number
K201895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5891
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cefaly Technology
Date Received
July 8, 2020
Decision Date
September 29, 2020
Product Code
PCC
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PCC Stimulator, Nerve, Electrical, Transcutaneous, For Migraine

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PCC), ordered by most recent decision date.

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Other Clearances by Cefaly Technology

K Number Device Name
K234029 CEFALY Connected - OTC, CEFALY Connected - Rx
K212071 Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx, Cefaly Dual Connected - OTC, Cefaly Dual Connected - Rx
K173006 Cefaly Dual
K171446 Cefaly Acute
K160237 Cefaly