Wallenstein Medium Slant

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K880138 ↗

FDA Product Code

KZI

Device Class

Class I

Regulation

21 CFR Part 866.2330

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Xylose Lysine Deoxycholate Agar

  Class I

  FDA 510(k) K821605 Active Cleared 6 Jul 1982

• Lysine Iron Agar Lia

  Class I

  FDA 510(k) K850548 Active Cleared 11 Mar 1985

• Bacteroides Bile Esculin Agar

  Class I

  FDA 510(k) K870638 Active Cleared 14 Apr 1987

• Brilliant Green Bile Broth

  Class I

  FDA 510(k) K880129 Active Cleared 30 Mar 1988

• Eosin Methylene Blue Agar (Levine)

  Class I

  FDA 510(k) K811642 Active Cleared 2 Jul 1981

• Ats Media

  Class I

  FDA 510(k) K880130 Active Cleared 30 Mar 1988

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