STRYKER MPS ACUTE CARE BED

STRYKER MPS ACUTE CARE BED is an FDA 510(k)-cleared medical device (K931482) manufactured by Stryker Corp.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 8, 1993. Regulation: 8.