GASLINE FILTER, #EC-GLF SERIES

GASLINE FILTER, #EC-GLF SERIES is an FDA 510(k)-cleared medical device (K832935) manufactured by Gish Biomedical, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 21, 1983. Regulation: 8.