REGENT BIOGEL DIAG PROCED GLOVES HYPOALLERG CLAIMS

REGENT BIOGEL DIAG PROCED GLOVES HYPOALLERG CLAIMS is an FDA 510(k)-cleared medical device (K902601) manufactured by Regent Hospital Products. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 9, 1990. Regulation: 8.