DWFritz ASM2000

DWFritz ASM2000 is an FDA 510(k)-cleared medical device (K213894) manufactured by Dwfritz Automation, Inc.. 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 13, 2022. Regulation: 8.