Abuscreen Fp for Cannabinoids (50-100)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K910589 ↗

FDA Product Code

LDJ

Device Class

Class II

Regulation

21 CFR Part 862.3870

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

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  Class II

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  Class I

  FDA 510(k) K962231 Active Cleared 30 Aug 1996

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  Class I

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  FDA 510(k) K962411 Active Cleared 7 Oct 1996

See all devices from Roche Diagnostic Systems, Inc. →