EQUI-PISE 1000 MRS

EQUI-PISE 1000 MRS is an FDA 510(k)-cleared medical device (K970350) manufactured by Advanced Air Support Consultancy, 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 April 21, 1997. Regulation: 8.