AP900/PRP MODULE AND ACCESSORIES, MODIFICATION

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION is an FDA 510(k)-cleared medical device (K893218) manufactured by Electromedics, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 11, 1990. Regulation: 8.