Kenlor Liquid Urine Control

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K890577 ↗

FDA Product Code

JJW

Device Class

Class I

Regulation

21 CFR Part 862.1660

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Kenlor Liquid Total Urine Control

  Class I

  FDA 510(k) K952840 Active Cleared 19 Jul 1995

• Kenlor Human Spinal Fluid Control

  Class I

  FDA 510(k) K950326 Active Cleared 20 Mar 1995

• Kenlor Total Iron, Uibc/Tibc Assay Kit

  Class I

  FDA 510(k) K890573 Active Cleared 24 Mar 1989

• Kenlor Human Spinal Fluid Control Liquid

  Class I

  FDA 510(k) K890576 Active Cleared 9 Mar 1989

• Kenlor Pyrogallol Red Microprotein Assay Kit

  Class I

  FDA 510(k) K896440 Active Cleared 16 Feb 1990

• Kenlor Therapeutic Drug Monitoring (Tdm) Control

  Class I

  FDA 510(k) K903338 Active Cleared 7 Sep 1990

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