AIM-V (R) MEDIUM, MODEL 087-0112

AIM-V (R) MEDIUM, MODEL 087-0112 is an FDA 510(k)-cleared medical device (K022086) manufactured by Invitrogen Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 22, 2002. Regulation: 8.