Rat Liver Nuclei Test System

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

510(k) Number

K870732 ↗

FDA Product Code

DHN

Device Class

Class II

Regulation

21 CFR Part 866.5100

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

• Histo-Check Legionella Control Slides

  Class I

  FDA 510(k) K883567 Active Cleared 6 Oct 1988

• Dual Substrate Ana

  Class II

  FDA 510(k) K871395 Active Cleared 20 Apr 1987

• Histo-Check Fungal Control Slides

  Class I

  FDA 510(k) K883570 Active Cleared 6 Oct 1988

• Histo-Check Gram Negative Slides

  Class I

  FDA 510(k) K883569 Active Cleared 6 Oct 1988

• Histo-Check Acid Fast Slides

  Class I

  FDA 510(k) K883568 Active Cleared 6 Oct 1988

• Herpes Virus Control Slides

  Class II

  FDA 510(k) K883684 Active Cleared 28 Sep 1988

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