K-number	K003577
Device name	STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT
Applicant	STERIS Corporation
Product code	FST
Device class	Class II
Decision date	Jan 29, 2001
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT

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