LAPAROBAG(TM) TISSUE RETRIEVAL SYSTEM

LAPAROBAG(TM) TISSUE RETRIEVAL SYSTEM is an FDA 510(k)-cleared medical device (K914547) manufactured by Baxter Healthcare Corp. 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 November 21, 1991. Regulation: 8.