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The [[United States of America|United States]] [[Food and Drug Administration]] classifies these systems as [[medical device]]s, under the general instrumentation category of [[automatic test equipment]].<ref>{{cite book|url=https://books.google.com/books?id=nEHLxh9wxZIC&pg=PA80&lpg=PA80&dq=%22FDA+automatic+test+equipment%22 |title=Testing Computer Systems for FDA/MHRA Compliance - David Stokes - Google Books |publisher=Books.google.com |date= 2003-11-25|accessdate=2012-07-12|isbn=9780849321634}}</ref>
ATIS have seven basic processes (sample preparation, image acquisition, image analysis, results reporting, data storage, network communication, and self-system diagnostics) and realization of these functions highly accurate hardware and well-integrated, complex, and expensive software.<ref>{{cite journal|doi=10.1016/j.aca.2005.11.083 |title=Analytica Chimica Acta - Advances in cancer tissue microarray technology: Towards improved understanding and diagnostics |date= | volume=564 |journal=Analytica Chimica Acta |pages=74–81|pmc=2583100}}</ref>
===Preparation===
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