NEEDLE, ASPIRATION & INJECTION, DISPOSABLE

NEEDLE, ASPIRATION & INJECTION, DISPOSABLE is an FDA 510(k)-cleared medical device (K902422) manufactured by Gainor Medical Europe, Ltd.. 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 5, 1991. Regulation: 8.