ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS

ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS is an FDA 510(k)-cleared medical device (K133604) manufactured by The Anspach Effort, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 9, 2014. Regulation: 8.