PAJUNK MODULAR HANDLE INSTRUMENTS

PAJUNK MODULAR HANDLE INSTRUMENTS is an FDA 510(k)-cleared medical device (K033249) manufactured by Pajunk GmbH. 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 March 4, 2004. Regulation: 8.