IL TEST(TM) AMPHETAMINE— 510(k) K913738

Name: FDA 510(k) clearance K913738
Creator: U.S. Food and Drug Administration
Published: 1991-11-07

Substantially Equivalent

Instrumentation Laboratory CO

FDA 510(k) clearance K913738 for IL TEST(TM) AMPHETAMINE, Substantially Equivalent on 1991-11-07. Applicant: Instrumentation Laboratory CO. Device class: 2.

Clearance details

Applicant: Instrumentation Laboratory CO
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1991-08-20
Decision date: 1991-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lexington, MA, US

Download summary PDF View on FDA.gov ↗

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