LKB 2161 MIDISPIN R CENTRIFUGE

LKB 2161 MIDISPIN R CENTRIFUGE is an FDA 510(k)-cleared medical device (K831948) 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.