CULTURETTE BRAND RAPID LATEX TEST CLOSTRIDIUM TOXI

CULTURETTE BRAND RAPID LATEX TEST CLOSTRIDIUM TOXI is an FDA 510(k)-cleared medical device (K852044) manufactured by Marion Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 18, 1985. Regulation: 8.