Complement-Fixation Test for Campylobacter Jejuni

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K862814 ↗

FDA Product Code

LQP

FDA applicant

Institute Virion , Ltd.

Device Class

Class I

Regulation

21 CFR Part 866.3110

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• H. Simplex Virus

  Class II

  FDA 510(k) K843658 Active Cleared 26 Sep 1985

• Chlamydia

  Class I

  FDA 510(k) K843654 Active Cleared 8 Aug 1985

• Influenza A2 Virus

  Class I

  FDA 510(k) K843659 Active Cleared 26 Sep 1985

• Adenovirus

  Class I

  FDA 510(k) K843649 Active Cleared 26 Sep 1985

• In Fluenza B Virus

  Class I

  FDA 510(k) K843660 Active Cleared 26 Sep 1985

• Mycoplasma Pneumoniae

  Class I

  FDA 510(k) K843664 Active Cleared 25 Oct 1984

See all devices from Institute Virion, Ltd. →