AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY is an FDA 510(k)-cleared medical device (K010752) manufactured by Aesculap, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 10, 2001. Regulation: 8.