Toxoplasma Gondii Igg Elisa

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K871905 ↗

FDA Product Code

LGD

Device Class

Class II

Regulation

21 CFR Part 866.3780

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Lipase Hydrolysis/Glycerol Kinase, Triglycerides

  Class I

  FDA 510(k) K863874 Active Cleared 13 Nov 1986

• Gemeni Igm Assay

  Class II

  FDA 510(k) K800450 Active Cleared 24 Apr 1980

• Herpes Ident. & Typing Test Hitt

  Class II

  FDA 510(k) K831504 Active Cleared 20 Sep 1983

• Gemeni Igg Assay

  Class II

  FDA 510(k) K800451 Active Cleared 24 Apr 1980

• Gemstar System

  Class I

  FDA 510(k) K821335 Active Cleared 13 Jul 1982

• Antibody to Herpesvirus Hominis

  Class II

  FDA 510(k) K791058 Active Cleared 7 Sep 1979

See all devices from Electro-Nucleonics Laboratories, Inc. →