Enriched Culture Med. Tryptic Soy Agar

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K841838 ↗

FDA Product Code

KZI

Device Class

Class I

Regulation

21 CFR Part 866.2330

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Culture Medium for Pathogenic Neisser

  Class II

  FDA 510(k) K841833 Active Cleared 14 May 1984

• Differential Culture Medium-Biggy Agar

  Class I

  FDA 510(k) K841844 Active Cleared 31 May 1984

• Enriched Culture Med. Fluid THIOGLYC0

  Class I

  FDA 510(k) K841837 Active Cleared 21 May 1984

• Selective Culture Med. Columbia Cna

  Class I

  FDA 510(k) K841845 Active Cleared 31 May 1984

• Selective Culture Med. Phenylethyl Alco

  Class I

  FDA 510(k) K841840 Active Cleared 25 May 1984

• Selective Culture Med. Trichomonas

  Class I

  FDA 510(k) K841836 Active Cleared 14 May 1984

See all devices from Microline Scientific →