AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III— 510(k) K050186

Substantially Equivalent

Ameditech, Inc.

FDA 510(k) clearance K050186 for AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III, Substantially Equivalent on 2005-03-04. Applicant: Ameditech, Inc..

Clearance details

Applicant: Ameditech, Inc.
Product code: Code DKZ
Advisory panel: Clinical Toxicology
Date received: 2005-01-27
Decision date: 2005-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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