FINGERPRINT DRUG SCREENING DEVICE— 510(k) K973726

Name: FDA 510(k) clearance K973726
Creator: U.S. Food and Drug Administration
Published: 1997-11-06

Substantially Equivalent

Applied Technology Ventures, LLC

FDA 510(k) clearance K973726 for FINGERPRINT DRUG SCREENING DEVICE, Substantially Equivalent on 1997-11-06. Applicant: Applied Technology Ventures, LLC. Device class: 2.

Clearance details

Applicant: Applied Technology Ventures, LLC
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1997-09-30
Decision date: 1997-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

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