Wright-Giemsa Quick Stain

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K842745 ↗

FDA Product Code

IAF

Device Class

Class I

Regulation

21 CFR Part 864.1850

Advisory Committee

Hematology

FDA Decision

SESE Substantially Equivalent

• Pap Stain, Ea-36

  Class I

  FDA 510(k) K842739 Active Cleared 11 Sep 1984

• Wright Stain Fixative

  Class I

  FDA 510(k) K842913 Active Cleared 7 Sep 1984

• Muci-Carmine Stain, Mayer's Formula

  Class I

  FDA 510(k) K842925 Active Cleared 11 Sep 1984

• Drabkin Reagent

  Class I

  FDA 510(k) K842931 Active Cleared 21 Sep 1984

• Picric Acid Saturated Solution

  Class I

  FDA 510(k) K842922 Active Cleared 7 Sep 1984

• Supermount

  Class I

  FDA 510(k) K842727 Active Cleared 3 Aug 1984

See all devices from E K Ind., Inc. →