KENLOR H. PYLORI CONTROL SERUM

KENLOR H. PYLORI CONTROL SERUM is an FDA 510(k)-cleared medical device (K964014) manufactured by Kenlor Industries, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 2, 1997. Regulation: 8.