Deoxycholate Citrate Agar

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K833204 ↗

FDA Product Code

JSI

Device Class

Class I

Regulation

21 CFR Part 866.2360

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Acu-Desoxycholate Agar

  Class I

  FDA 510(k) K811134 Active Cleared 5 May 1981

• Thioglycollate Medium W/Out Indicator

  Class I

  FDA 510(k) K811340 Active Cleared 29 May 1981

• Lactabacillus Agar W/O TWEEN80

  Not classified

  FDA 510(k) K833292 Active Cleared 14 Nov 1983

• Bile Salts Mixture

  Class I

  FDA 510(k) K833211 Active Cleared 27 Oct 1983

• Eugon Broth

  Class I

  FDA 510(k) K811132 Active Cleared 5 May 1981

• Amies Transport Medium

  Class I

  FDA 510(k) K881539 Active Cleared 18 Apr 1988

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