SelectFlex 072 Neurovascular Access System

SelectFlex 072 Neurovascular Access System is an FDA 510(k)-cleared medical device (K181000) manufactured by Q'Apel. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 12, 2018. Regulation: 8.