SUPERJET DISPOSABLE BLOOD LANCET

SUPERJET DISPOSABLE BLOOD LANCET is an FDA 510(k)-cleared medical device (K833812) manufactured by Medrobe Laboratories. 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 December 11, 1983. Regulation: 8.