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510(k) K203419

Relivion by Neurolief , Ltd. — Product Code PCC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 2021
Date Received
November 19, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Nerve, Electrical, Transcutaneous, For Migraine
Device Class
Class II
Regulation Number
882.5891
Review Panel
NE
Submission Type

Used to apply an electrical current to a patient's cranium through electrodes placed on the skin.

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