COAST MEDICAL, INC. RECTAL PROBE

COAST MEDICAL, INC. RECTAL PROBE is an FDA 510(k)-cleared medical device (K930930) manufactured by Coast Medical 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 February 24, 1994. Regulation: 8.