510(k) K170435

NerveGuard NRFit, NerveGuard LUER by PAJUNK GmbH Medizintechnologie — Product Code BSP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 2017
Date Received
February 13, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
Device Class
Class II
Regulation Number
868.5150
Review Panel
AN
Submission Type