FDA 510(k), K042912, INTERX5000
FDA 510(k), K042912, INTERX5000
Device Name: INTERX5000
Manufacturer:
Device Classification Name: Stimulator, Nerve, Transcutaneous, For Pain Relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 10/21/2004
Decision Date: 05/17/2005
Regulation Medical Specialty: Neurology
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