HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500

HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500 is an FDA 510(k)-cleared medical device (K041280) manufactured by Felton International, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 23, 2004. Regulation: 8.