ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM

ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM is an FDA 510(k)-cleared medical device (K972406) manufactured by Immunoprobe, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 21, 1997. Regulation: 8.