URINE SPECIMEN CONTAINER #'S 1013-1016

URINE SPECIMEN CONTAINER #'S 1013-1016 is an FDA 510(k)-cleared medical device (K802002) manufactured by Pollak (Intl.), Ltd.. This device is classified under the Pathology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 8, 1980. Regulation: 8.