HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA)

HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA) is an FDA 510(k)-cleared medical device (K862555) manufactured by Viromed Laboratories, Inc.. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 9, 1986. Regulation: 8.