NO STEP ON SITE DEUG TEST CUP— 510(k) K012390

Name: FDA 510(k) clearance K012390
Creator: U.S. Food and Drug Administration
Published: 2001-12-18

Substantially Equivalent

Drug Free Enterprises

FDA 510(k) clearance K012390 for NO STEP ON SITE DEUG TEST CUP, Substantially Equivalent on 2001-12-18. Applicant: Drug Free Enterprises. Device class: 2.

Clearance details

Applicant: Drug Free Enterprises
Product code: Code LDJ
Device class: Class 2
Regulation: 21 CFR 862.3870
Advisory panel: Clinical Toxicology
Date received: 2001-07-27
Decision date: 2001-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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