Adpifa Test for Antibodies to Toxoplasma Gondii

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K844287 ↗

FDA Product Code

GLZ

Device Class

Class II

Regulation

21 CFR Part 866.3780

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Adp Ndna Ifa Test

  Class II

  FDA 510(k) K842707 Active Cleared 21 Aug 1984

• Adp Ana Ifa Test

  Class II

  FDA 510(k) K842183 Active Cleared 22 Jun 1984

• Adp Ana Applezyme

  Class II

  FDA 510(k) K843745 Active Cleared 25 Oct 1984

• Adp Ifa Test for Chlamydiae Trachomatis

  Class I

  FDA 510(k) K834242 Active Cleared 2 Mar 1984

• Ana Applelisa

  Class II

  FDA 510(k) K834241 Active Cleared 4 Apr 1984

• Applelisa Chlamydia Trachomatis Anti

  Class I

  FDA 510(k) K843120 Active Cleared 12 Sep 1984