Leeco Testosterone Diagnostic Kit

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

510(k) Number

K860003 ↗

FDA Product Code

CDZ

Device Class

Class I

Regulation

21 CFR Part 862.1680

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K870259 Active Cleared 10 Mar 1987

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  Class I

  FDA 510(k) K854838 Active Cleared 7 Jan 1986

• Leeco Ferritin-Quant Diag. Test Kit

  Class II

  FDA 510(k) K811880 Active Cleared 16 Jul 1981

• Leeco Fsh-Quant Diagnostic Kit

  Class I

  FDA 510(k) K810663 Active Cleared 27 Mar 1981

• Leeco Glyco-Hemoglobin Diag. Test Kit

  Class II

  FDA 510(k) K801289 Active Cleared 30 Jun 1980

• Leeco Prl-Quant Diagnostic Test Kit

  Class I

  FDA 510(k) K820039 Active Cleared 22 Jan 1982

See all devices from Leeco Diagnostics, Inc. →