ABUSCREEN (R) EIA BARBITURATE— 510(k) K870378

Substantially Equivalent

Roche Diagnostic Systems, Inc.

FDA 510(k) clearance K870378 for ABUSCREEN (R) EIA BARBITURATE, Substantially Equivalent on 1987-03-16. Applicant: Roche Diagnostic Systems, Inc..

Clearance details

Applicant: Roche Diagnostic Systems, Inc.
Product code: Code DIS
Advisory panel: Clinical Toxicology
Date received: 1987-01-29
Decision date: 1987-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nutley, NJ, US

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