USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200— 510(k) K932318

Name: FDA 510(k) clearance K932318
Creator: U.S. Food and Drug Administration
Published: 1993-06-15

Substantially Equivalent

U.S. Drug Testing, Inc.

FDA 510(k) clearance K932318 for USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200, Substantially Equivalent on 1993-06-15. Applicant: U.S. Drug Testing, Inc.. Device class: 2.

Clearance details

Applicant: U.S. Drug Testing, Inc.
Product code: Code DJG
Device class: Class 2
Regulation: 21 CFR 862.3650
Advisory panel: Clinical Toxicology
Date received: 1993-05-11
Decision date: 1993-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rancho Cucamonga, CA, US

Download summary PDF View on FDA.gov ↗

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