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FDA 510(k), K180222, Reaxon Plus
FDA 510(k), K180222, Reaxon Plus
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$49.00 USD
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510(K) Number: K180222
Device Name: Reaxon Plus
Manufacturer: Medovent GmbH
Device Classification Name: cuff, nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 01/25/2018
Decision Date: 04/24/2018
Regulation Medical Specialty: Neurology
Device Name: Reaxon Plus
Manufacturer: Medovent GmbH
Device Classification Name: cuff, nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 01/25/2018
Decision Date: 04/24/2018
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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