MONOJECT(R) MONOLETTOR SAFETY LANCET

MONOJECT(R) MONOLETTOR SAFETY LANCET is an FDA 510(k)-cleared medical device (K932785) manufactured by Sherwood Medical Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 28, 1993. Regulation: 8.