HYCOR PYLORAGEN HELICOBACTER PYLORI TEST

HYCOR PYLORAGEN HELICOBACTER PYLORI TEST is an FDA 510(k)-cleared medical device (K912255) manufactured by Hycor Biomedical, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 10, 1991. Regulation: 8.