K-number	K130542
Device name	SYNAPSE 3D LUNG AND ABDOMEN ANALYSIS
Applicant	Fujifilm Medical System U.S.A., Inc.
Product code	LLZ
Device class	Class II
Decision date	Jun 14, 2013
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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SYNAPSE 3D LUNG AND ABDOMEN ANALYSIS

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