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FDA 510(k), K170435, NerveGuard NRFit, NerveGuard LUER
FDA 510(k), K170435, NerveGuard NRFit, NerveGuard LUER
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$149.00 USD
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$149.00 USD
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510(K) Number: K170435
Device Name: NerveGuard NRFit, NerveGuard LUER
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation Number: 868.5150
Classification Product Code: BSP
Date Received: 02/13/2017
Decision Date: 07/12/2017
Regulation Medical Specialty: Anesthesiology
Device Name: NerveGuard NRFit, NerveGuard LUER
Manufacturer: PAJUNK GmbH Medizintechnologie
Device Classification Name: Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation Number: 868.5150
Classification Product Code: BSP
Date Received: 02/13/2017
Decision Date: 07/12/2017
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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