KDI QUIK TEST(TM) MARIJUANA SCREEN— 510(k) K870197

Name: FDA 510(k) clearance K870197
Creator: U.S. Food and Drug Administration
Published: 1987-06-01

Substantially Equivalent

Keystone Diagnostics, Inc.

FDA 510(k) clearance K870197 for KDI QUIK TEST(TM) MARIJUANA SCREEN, Substantially Equivalent on 1987-06-01. Applicant: Keystone Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Keystone Diagnostics, Inc.
Product code: Code LDJ
Device class: Class 2
Regulation: 21 CFR 862.3870
Advisory panel: Clinical Toxicology
Date received: 1987-01-20
Decision date: 1987-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.