DRUGCHECK X MULTIDRUG SCREENING DEVICE— 510(k) K992748

Name: FDA 510(k) clearance K992748
Creator: U.S. Food and Drug Administration
Published: 1999-09-02

Substantially Equivalent

Syntron Bioresearch, Inc.

FDA 510(k) clearance K992748 for DRUGCHECK X MULTIDRUG SCREENING DEVICE, Substantially Equivalent on 1999-09-02. Applicant: Syntron Bioresearch, Inc.. Device class: 2.

Clearance details

Applicant: Syntron Bioresearch, Inc.
Product code: Code DIO
Device class: Class 2
Regulation: 21 CFR 862.3250
Advisory panel: Clinical Toxicology
Date received: 1999-08-16
Decision date: 1999-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Simi Valley, CA, US

Download summary PDF View on FDA.gov ↗

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