LKB-BROMMA 2218 HISTORANGE MICROTOME

LKB-BROMMA 2218 HISTORANGE MICROTOME is an FDA 510(k)-cleared medical device (K812157) manufactured by Lkb Instruments, Inc.. This device is classified under the Pathology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 17, 1981. Regulation: 8.