NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM

NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM is an FDA 510(k)-cleared medical device (K042780) manufactured by Prosurg, Inc.. 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 February 2, 2005. Regulation: 8.