KLIGER'S IRON AGAR, SIM MEDIA, MRVP MEDIUM, BILE E

KLIGER'S IRON AGAR, SIM MEDIA, MRVP MEDIUM, BILE E is an FDA 510(k)-cleared medical device (K850721) manufactured by Rapid City Regional Hospital, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 21, 1985. Regulation: 8.