
Cordis Corp.
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BLOOD LINE COMP. NEG. PRESS. PILLOW is an FDA 510(k)-cleared medical device (K772355) manufactured by Cordis Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1978. Regulation: 8.