K-number	K943464
Device name	PHILIPS IMPROVED CHECK RADIOGRAPH OPTION
Applicant	Philips Medical Systems North America, Inc.
Product code	IYE
Device class	Class II
Decision date	Feb 1, 1995
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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PHILIPS IMPROVED CHECK RADIOGRAPH OPTION

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