CAPINTEC MODEL 292 ELECTROMETER

CAPINTEC MODEL 292 ELECTROMETER is an FDA 510(k)-cleared medical device (K980402) manufactured by Capintec, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 23, 1998. Regulation: 8.