This webinar is intended to demonstrate how to prepare a 510(k) in an adequate manner with increased quality to expedite the streamlined review process. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices.Price: $225.00USAGlobalCompliancePanel,Livermore Common, Fremont, CA, 94539USA Phone:800-447-9407Fax: 302-288-6884