K-number	K171355
Device name	Surefire Precision Infusion System
Applicant	Surefire Medical, Inc.
Product code	DQO
Device class	Class II
Decision date	May 17, 2017
Decision	Substantially Equivalent
Regulation	870.1200

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Source

View the full FDA submission: accessdata.fda.gov

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Surefire Precision Infusion System

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