Campylobacter Selective Agar

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K823307 ↗

FDA Product Code

JSI

Device Class

Class I

Regulation

21 CFR Part 866.2360

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Sxt Blood Agar

  Class I

  FDA 510(k) K832860 Active Cleared 26 Sep 1983

• Streptococcus Selective Agar

  Class I

  FDA 510(k) K823310 Active Cleared 15 Dec 1982

• Columbia V Agar W/5% Human Blood

  Class I

  FDA 510(k) K823311 Active Cleared 15 Dec 1982

• Dermotophyte Test Medium

  Class I

  FDA 510(k) K810181 Active Cleared 5 Feb 1981

• Sabouraud Dextrose Agar

  Class I

  FDA 510(k) K832861 Active Cleared 26 Sep 1983

• Bacti Plate (Dermatology) Product No. Ps-5000

  Class II

  FDA 510(k) K861301 Active Cleared 21 Apr 1986

See all devices from Troy Biologicals, Inc. →