K-number	K971455
Device name	CLARUS MODEL 5197 SIGHTLITE
Applicant	Clarus Medical Systems, Inc.
Product code	FTI
Device class	Class II
Decision date	May 20, 1997
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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CLARUS MODEL 5197 SIGHTLITE

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