PSEUDOMONAS AGAR P (MEDIUM A)

PSEUDOMONAS AGAR P (MEDIUM A) is an FDA 510(k)-cleared medical device (K860750) 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 March 9, 1986. Regulation: 8.