MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES

MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES is an FDA 510(k)-cleared medical device (K142022) manufactured by Medline Renewal. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 18, 2014. Regulation: 8.