K-number	K082306
Device name	POWERLOC CLEAR SAFETY INFUSION SET
Applicant	C.R. Bard, Inc.
Product code	FPA
Device class	Class II
Decision date	Aug 28, 2008
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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POWERLOC CLEAR SAFETY INFUSION SET

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