Brucella Media

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K834006 ↗

FDA Product Code

JSG

Device Class

Class I

Regulation

21 CFR Part 866.2300

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Columbia Agar Cna W/5% Sheep Blood

  Class I

  FDA 510(k) K811607 Active Cleared 25 Jun 1981

• Bile Esculin Media

  Class I

  FDA 510(k) K811600 Active Cleared 25 Jun 1981

• Thioglycolate Medium W/Vitamin Kl & Hemin

  Class I

  FDA 510(k) K850847 Active Cleared 20 Mar 1985

• Eosin Methylene Blue Agar (Levine)

  Class I

  FDA 510(k) K811610 Active Cleared 25 Jun 1981

• Bacteriological Culture Media

  Class I

  FDA 510(k) K790497 Active Cleared 10 Apr 1979

• Brain Heart Infusion Agar

  Class I

  FDA 510(k) K850848 Active Cleared 20 Mar 1985

See all devices from Micro Media Laboratories →