Mueller Hinton Medium

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K854451 ↗

FDA Product Code

JTZ

Device Class

Class II

Regulation

21 CFR Part 866.1700

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Columbia Cna Agar W/5% Sheep Blood

  Class I

  FDA 510(k) K854457 Active Cleared 18 Nov 1985

• Tryptic Soy Blood Agar

  Class I

  FDA 510(k) K854454 Active Cleared 18 Nov 1985

• Chlamydia & Viral Transport Medium

  Class I

  FDA 510(k) K871065 Active Cleared 14 Apr 1987

• Cdc Anaerobe Blood Agar

  Class I

  FDA 510(k) K854455 Active Cleared 18 Nov 1985

• Columbia 5% Blood Agar

  Class I

  FDA 510(k) K854228 Active Cleared 31 Oct 1985

• Thayer-Martin Medium (Mod)

  Class II

  FDA 510(k) K854275 Active Cleared 12 Nov 1985

See all devices from R. Kent Richards, Inc. →