K-number	K050866
Device name	CENTRION 500 C-ARM SYSTEM
Applicant	Osteosys Co.,Ltd
Product code	JAA
Device class	Class II
Decision date	Apr 27, 2005
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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CENTRION 500 C-ARM SYSTEM

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