Hektoen Enteric Agar

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K841745 ↗

FDA Product Code

JSI

Device Class

Class I

Regulation

21 CFR Part 866.2360

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Salmonella-Shigella Agar

  Class I

  FDA 510(k) K841746 Active Cleared 31 May 1984

• Macconkey Agar

  Class I

  FDA 510(k) K841753 Active Cleared 7 Jun 1984

• Levine Eosin Methylene Blue Agar

  Class I

  FDA 510(k) K841751 Active Cleared 31 May 1984

• Sheep Blood Agar

  Class I

  FDA 510(k) K841748 Active Cleared 31 May 1984

• Xylose-Lysine Desoxycholate Agar

  Class I

  FDA 510(k) K841752 Active Cleared 7 Jun 1984

• Columbia Cna Agar

  Class I

  FDA 510(k) K841754 Active Cleared 7 May 1984

See all devices from The Montana Deaconess Medical Center →