HEKTOEN ENTERIC (HE) AGAR PRODUCT #P3330

HEKTOEN ENTERIC (HE) AGAR PRODUCT #P3330 is an FDA 510(k)-cleared medical device (K873329) manufactured by Lakewood Biochemical Co., Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 1, 1987. Regulation: 8.