VOLKER HOSPITAL BED, MODEL K960

VOLKER HOSPITAL BED, MODEL K960 is an FDA 510(k)-cleared medical device (K972115) manufactured by Volker Healthcare, Inc.. 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 August 28, 1997. Regulation: 8.