ABUSCREEN(R) RADIOIMMUNOASSAY FOR METHAMPHE/AMPHET— 510(k) K913911

Substantially Equivalent

Roche Diagnostic Systems, Inc.

FDA 510(k) clearance K913911 for ABUSCREEN(R) RADIOIMMUNOASSAY FOR METHAMPHE/AMPHET, Substantially Equivalent on 1991-11-01. Applicant: Roche Diagnostic Systems, Inc..

Clearance details

Applicant: Roche Diagnostic Systems, Inc.
Product code: Code DPJ
Advisory panel: Clinical Toxicology
Date received: 1991-08-30
Decision date: 1991-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montclair, NJ, US

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