510(k) K171802

ALEVE Direct Therapy (ALEVE Direct Therapy TENS Device) by Bayer Healthcare, LLC — Product Code NUH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 2018
Date Received
June 19, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Nerve, Transcutaneous, Over-The-Counter
Device Class
Class II
Regulation Number
882.5890
Review Panel
NE
Submission Type

TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES