Herpes Simplex Virus Serological Reagent

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

510(k) Number

K803132 ↗

FDA Product Code

GQL

Device Class

Class II

Regulation

21 CFR Part 866.3305

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• The Golden Quad Test (Ebv)

  Class I

  FDA 510(k) K861121 Active Cleared 2 Feb 1987

• Rubella Virus Serological Reagents

  Class II

  FDA 510(k) K803175 Active Cleared 29 Jan 1981

• Cmv Test

  Class II

  FDA 510(k) K843138 Active Cleared 29 Jan 1985

• The Golden Quad Test (Toxo)

  Class II

  FDA 510(k) K861122 Active Cleared 2 Feb 1987

• Antihuman Igg Globulin Fitc Labeled

  Class II

  FDA 510(k) K821018 Active Cleared 29 Apr 1982

• Toxoplasma Gondii Serological Reagents

  Class II

  FDA 510(k) K803134 Active Cleared 29 Jan 1981

See all devices from Microbiological Research Corp. →