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FDA 510(k), K062616, WELLNESSPRO 2010
FDA 510(k), K062616, WELLNESSPRO 2010
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510(K) Number: K062616
Device Name: WELLNESSPRO 2010
Manufacturer: INTELSOURCE GROUP, INC.
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 09/05/2006
Decision Date: 07/06/2007
Regulation Medical Specialty: Neurology
Device Name: WELLNESSPRO 2010
Manufacturer: INTELSOURCE GROUP, INC.
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 09/05/2006
Decision Date: 07/06/2007
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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