K-number	K150565
Device name	Supria Whole-body X-ray CT System
Applicant	Hitachi Medical Systems America, Inc.
Product code	JAK
Device class	Class II
Decision date	Sep 30, 2015
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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Supria Whole-body X-ray CT System

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