NanoKnife Generator (H78720300351US0)

NanoKnife Generator (H78720300351US0) is an FDA 510(k)-cleared medical device (K253198) manufactured by Angiodynamics. 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 March 23, 2026. Regulation: 8.