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FDA 510(k), K111576, NT 2000 LESIONING GENERATOR
FDA 510(k), K111576, NT 2000 LESIONING GENERATOR
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510(K) Number: K111576
Device Name: NT 2000 LESIONING GENERATOR
Manufacturer: NEUROTHERM, INC.
Device Classification Name: generator, lesion, radiofrequency
Regulation Number: 882.4400
Classification Product Code: GXD
Date Received: 06/06/2011
Decision Date: 09/20/2011
Regulation Medical Specialty: Neurology
Device Name: NT 2000 LESIONING GENERATOR
Manufacturer: NEUROTHERM, INC.
Device Classification Name: generator, lesion, radiofrequency
Regulation Number: 882.4400
Classification Product Code: GXD
Date Received: 06/06/2011
Decision Date: 09/20/2011
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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