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FDA 510(k), K173233, ReliefBand 1.5
FDA 510(k), K173233, ReliefBand 1.5
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$149.00 USD
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510(K) Number: K173233
Device Name: ReliefBand 1.5
Manufacturer: ReliefBand Technologies
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 10/05/2017
Decision Date: 11/30/2017
Regulation Medical Specialty: Neurology
Device Name: ReliefBand 1.5
Manufacturer: ReliefBand Technologies
Device Classification Name: stimulator, nerve, transcutaneous, for pain relief
Regulation Number: 882.5890
Classification Product Code: GZJ
Date Received: 10/05/2017
Decision Date: 11/30/2017
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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