KONICA LASER IMAGER LI-21

KONICA LASER IMAGER LI-21 is an FDA 510(k)-cleared medical device (K950359) manufactured by Storch Amini & Munves PC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 5, 1995. Regulation: 8.