Cannulas for Hema-Tek I & Kk Slide Stainers

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

510(k) Number

K850157 ↗

FDA Product Code

KPA

Device Class

Class I

Regulation

21 CFR Part 864.3800

Advisory Committee

Pathology

FDA Decision

SESE Substantially Equivalent

• Pump Tube Sets for Hema-Tek I & II Slide Stainers

  Class I

  FDA 510(k) K850333 Active Cleared 27 Feb 1985

• Potassium Analyzer-Sodium/Electrolyte

  Class II

  FDA 510(k) K830588 Active Cleared 27 Apr 1983

• Electrolyte Standard - Corning Nalk Ise

  Class II

  FDA 510(k) K830589 Active Cleared 27 Apr 1983

• Supplies for Instrumentation Lab Flame

  Class I

  FDA 510(k) K840530 Active Cleared 30 Mar 1984

• Shaban 9865 IL#78637 Junction Bloc

  Class I

  FDA 510(k) K833804 Active Cleared 13 Jan 1984

• External Standards-Sodiumnpotassium

  Class II

  FDA 510(k) K820700 Active Cleared 1 Apr 1982

See all devices from Shaban Mfg. Co. →