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FDA 510(k), K173861, Drug Relief
FDA 510(k), K173861, Drug Relief
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510(K) Number: K173861
Device Name: Drug Relief
Manufacturer: DyAnsys, Inc.
Device Classification Name: percutaneous nerve stimulator for opioid withdrawal
Regulation Number: 882.5896
Classification Product Code: PZR
Date Received: 12/20/2017
Decision Date: 05/02/2018
Regulation Medical Specialty: Neurology
Device Name: Drug Relief
Manufacturer: DyAnsys, Inc.
Device Classification Name: percutaneous nerve stimulator for opioid withdrawal
Regulation Number: 882.5896
Classification Product Code: PZR
Date Received: 12/20/2017
Decision Date: 05/02/2018
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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