PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES

PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES is an FDA 510(k)-cleared medical device (K994151) manufactured by Ximed/Prosure/Injectx. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 29, 2000. Regulation: 8.