DRI-FORM PSEUDOMONAS AGAR F

DRI-FORM PSEUDOMONAS AGAR F is an FDA 510(k)-cleared medical device (K852064) manufactured by Gibco Laboratories Life Technologies, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 3, 1985. Regulation: 8.