Enriched Culture Medium

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K850735 ↗

FDA Product Code

KZI

Device Class

Class I

Regulation

21 CFR Part 866.2330

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Transport Culture Medium

  Class I

  FDA 510(k) K850737 Active Cleared 20 Mar 1985

• Differential Culture Medium

  Class I

  FDA 510(k) K850734 Active Cleared 20 Mar 1985

• Culture Medium for Pathogenic Neisseria Ssp.mi

  Class II

  FDA 510(k) K850732 Active Cleared 20 Mar 1985

• Supplement for Culture Medium

  Class I

  FDA 510(k) K850738 Active Cleared 20 Mar 1985

• Multipurpose Culture Medium

  Class I

  FDA 510(k) K850733 Active Cleared 20 Mar 1985

• Selective Culture Medium

  Class I

  FDA 510(k) K850736 Active Cleared 20 Mar 1985

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