ANSPACH ANGLED MICRONOSE ATTACHMENT

ANSPACH ANGLED MICRONOSE ATTACHMENT is an FDA 510(k)-cleared medical device (K002903) 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 October 23, 2000. Regulation: 8.