CANNABINOID ASSAY AND THE RANDOX CANNABINOID CALIBRATOR/ CONTROL SET— 510(k) K092269

Substantially Equivalent

Randox Laboratories, Ltd.

FDA 510(k) clearance K092269 for CANNABINOID ASSAY AND THE RANDOX CANNABINOID CALIBRATOR/ CONTROL SET, Substantially Equivalent on 2011-04-08. Applicant: Randox Laboratories, Ltd..

Clearance details

Applicant: Randox Laboratories, Ltd.
Product code: Code LDJ
Advisory panel: Clinical Toxicology
Date received: 2009-07-28
Decision date: 2011-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crumlin, GB

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