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FDA 510(k), K160295, SPROTTE NRFit, Quincke NRFit
FDA 510(k), K160295, SPROTTE NRFit, Quincke NRFit
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$149.00 USD
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$149.00 USD
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510(K) Number: K160295
Device Name: SPROTTE NRFit, Quincke NRFit
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: needle, conduction, anesthetic (w/wo introducer)
Regulation Number: 868.5150
Classification Product Code: BSP
Date Received: 02/03/2016
Decision Date: 10/27/2016
Regulation Medical Specialty: Anesthesiology
Device Name: SPROTTE NRFit, Quincke NRFit
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: needle, conduction, anesthetic (w/wo introducer)
Regulation Number: 868.5150
Classification Product Code: BSP
Date Received: 02/03/2016
Decision Date: 10/27/2016
Regulation Medical Specialty: Anesthesiology
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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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