POLYESTER SPONGE PATTIE

POLYESTER SPONGE PATTIE is an FDA 510(k)-cleared medical device (K862494) manufactured by American Silk Sutures, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 29, 1986. Regulation: 8.