K-number	K101708
Device name	PATIENT SAFE LUER CAP
Applicant	Retractable Technologies, Inc.
Product code	FMF
Device class	Class II
Decision date	Feb 24, 2011
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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PATIENT SAFE LUER CAP

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