RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER

RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER is an FDA 510(k)-cleared medical device (K073041) manufactured by Acclarent, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 10, 2008. Regulation: 8.