HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM

HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM is an FDA 510(k)-cleared medical device (K891456) manufactured by Baxter Healthcare Corp. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 1989. Regulation: 8.