SonoStik IV Guide Wire Introducer

SonoStik IV Guide Wire Introducer is an FDA 510(k)-cleared medical device (K152177) manufactured by Sonostik, LLC. 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 30, 2015. Regulation: 8.