EIA FOR DETECTION OF ANTIBODIES H. PYLORI

EIA FOR DETECTION OF ANTIBODIES H. PYLORI is an FDA 510(k)-cleared medical device (K905409) manufactured by E-Z-Em, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 9, 1991. Regulation: 8.