INTRABIONIC CO. - MICRO SYRINGE

INTRABIONIC CO. - MICRO SYRINGE is an FDA 510(k)-cleared medical device (K832350) manufactured by Intrabionic Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 27, 1983. Regulation: 8.