FDA 510(k) Application Details - K173233

Device Classification Name Stimulator, Nerve, Transcutaneous, For Pain Relief

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510(K) Number K173233
Device Name Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant ReliefBand Technologies
220 Gibraltar Rd Ste 270
Horsham, PA 19044 US
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Contact Dave Hartman
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Regulation Number 882.5890

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Classification Product Code GZJ
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Date Received 10/05/2017
Decision Date 11/30/2017
Decision SESE - SUBST EQUIV
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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