AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS

AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS is an FDA 510(k)-cleared medical device (K923133) manufactured by Microprobe Corp.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 24, 1992. Regulation: 8.