LKB 2160 MIDISPIN CENTRIFUGE

LKB 2160 MIDISPIN CENTRIFUGE is an FDA 510(k)-cleared medical device (K831947) manufactured by Lkb Instruments, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 28, 1983. Regulation: 8.