K-number	K073650
Device name	FUJIFILM UNITY SPEEDSUITE, MODEL CR-IR 371
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	KPR
Device class	Class II
Decision date	Feb 6, 2008
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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FUJIFILM UNITY SPEEDSUITE, MODEL CR-IR 371

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