DRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL— 510(k) K913650

Substantially Equivalent

Duo Research, Inc.

FDA 510(k) clearance K913650 for DRUG TESTING ASSESSMENT PROGRAM QUALITY CONTROL, Substantially Equivalent on 1991-09-06. Applicant: Duo Research, Inc..

Clearance details

Applicant: Duo Research, Inc.
Product code: Code DIF
Advisory panel: Clinical Toxicology
Date received: 1991-08-16
Decision date: 1991-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Annapolis, MD, US

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