CEDIA PROCAINAMIDE ASSAY

CEDIA PROCAINAMIDE ASSAY is an FDA 510(k)-cleared medical device (K962099) manufactured by Boehringer Mannheim Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1996. Regulation: 8.