K-number	K073423
Device name	MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER
Applicant	C.R. Bard, Inc.
Product code	LJT
Device class	Class II
Decision date	Dec 19, 2007
Decision	Substantially Equivalent
Regulation	880.5965

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View the full FDA submission: accessdata.fda.gov

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MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER

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