K-number	K090136
Device name	STERIS CMAX XLT SURGICAL TABLE
Applicant	STERIS Corporation
Product code	FQO
Device class	Class I
Decision date	Mar 20, 2009
Decision	Substantially Equivalent
Regulation	878.4960

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View the full FDA submission: accessdata.fda.gov

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STERIS CMAX XLT SURGICAL TABLE

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