K-number	K122661
Device name	VITAL 5 RELEAF CATHETER
Applicant	Vital 5
Product code	BSO
Device class	Class II
Decision date	Feb 27, 2013
Decision	Substantially Equivalent
Regulation	868.5120

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Source

View the full FDA submission: accessdata.fda.gov

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VITAL 5 RELEAF CATHETER

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