K-number	K962010
Device name	EPI-SCOPE OPTION FOR Q SERIES CT SYSTEMS
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	LLZ
Device class	Class II
Decision date	Mar 21, 1997
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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EPI-SCOPE OPTION FOR Q SERIES CT SYSTEMS

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