ULTRACELL INSTRUMENT WIPE

ULTRACELL INSTRUMENT WIPE is an FDA 510(k)-cleared medical device (K920353) manufactured by Ultracell Medical Technologies, 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 September 14, 1992. Regulation: 8.