Modified Thayer-Martin Agar (Plate)

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K791425 ↗

FDA Product Code

JTY

Device Class

Class II

Regulation

21 CFR Part 866.2410

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Mycological Agar W/Antibiotics

  Class I

  FDA 510(k) K844931 Active Cleared 27 Feb 1985

• Anaerobe Blood Agar

  Class I

  FDA 510(k) K820559 Active Cleared 19 Mar 1982

• Mannitol Salt Agar

  Class I

  FDA 510(k) K791621 Active Cleared 24 Sep 1979

• Levine Eosin Methyler

  Class I

  FDA 510(k) K791555 Active Cleared 17 Sep 1979

• Columbia Agar WITH5% Sheep

  Class I

  FDA 510(k) K791622 Active Cleared 24 Sep 1979

• Anaerobe Blood Agar W/Kanamycin & Vanco

  Class I

  FDA 510(k) K820555 Active Cleared 16 Mar 1982

See all devices from American Laboratory Supply, Inc. →