DRUGCHECK X MULTIDRUG SCREENING DEVICE— 510(k) K992748

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..

Clearance details

Applicant: Syntron Bioresearch, Inc.
Product code: Code DIO
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

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