ARTHROSCOPE,RIGID ROD-LENS DIAGNOSTIC ENDOSCOPE

ARTHROSCOPE,RIGID ROD-LENS DIAGNOSTIC ENDOSCOPE is an FDA 510(k)-cleared medical device (K943426) manufactured by Schoelly Technologies, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 31, 1995. Regulation: 8.