Antimicrobial Suscept-Culture Media

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K841213 ↗

FDA Product Code

JTZ

Device Class

Class II

Regulation

21 CFR Part 866.1700

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Non-Selective & Differential

  Class I

  FDA 510(k) K841206 Active Cleared 17 Apr 1984

• General Nutrient Broth

  Class I

  FDA 510(k) K841203 Active Cleared 4 Apr 1984

• Single Biochemical Test

  Class I

  FDA 510(k) K841212 Active Cleared 4 Apr 1984

• Propagating Transport

  Class I

  FDA 510(k) K841208 Active Cleared 5 Apr 1984

• Selective & Non-Differential

  Class I

  FDA 510(k) K841210 Active Cleared 4 Apr 1984

• Multiple Biochemical Test

  Class I

  FDA 510(k) K841204 Active Cleared 17 Apr 1984

See all devices from Smith River Biologicals →