FDA 510(k) Application Details - K840964

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

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510(K) Number K840964
Device Name Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant CODMAN & SHURTLEFF, INC.


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Regulation Number 882.5890

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Classification Product Code GZJ
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Date Received 03/06/1984
Decision Date 04/23/1984
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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