K-number	K890351
Device name	ORTHORALIX SD/ORTHORALIX SD CEPH
Applicant	Philips Medical Systems North America, Inc.
Product code	IZF
Device class	Class II
Decision date	Jun 15, 1989
Decision	Substantially Equivalent
Regulation	892.1740

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ORTHORALIX SD/ORTHORALIX SD CEPH

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