Cleared Traditional

K020769 - SINGLE ANALYTE URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS (FDA 510(k) Clearance)

Apr 2002
Decision
27d
Days
Class 2
Risk

K020769 is an FDA 510(k) clearance for the SINGLE ANALYTE URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS. This device is classified as a Calibrators, Drug Specific (Class II - Special Controls, product code DLJ).

Submitted by Lin-Zhi International, Inc. (San Jose, US). The FDA issued a Cleared decision on April 3, 2002, 27 days after receiving the submission on March 7, 2002.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3200.

Submission Details

510(k) Number K020769 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 2002
Decision Date April 03, 2002
Days to Decision 27 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF

Device Classification

Product Code DLJ — Calibrators, Drug Specific
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3200