K-number	K003122
Device name	SMARTFLOW, MODEL SFIP 2000
Applicant	Florence Medical , Ltd.
Product code	DSK
Device class	Class II
Decision date	May 14, 2001
Decision	Substantially Equivalent
Regulation	870.1110

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View the full FDA submission: accessdata.fda.gov

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SMARTFLOW, MODEL SFIP 2000

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