K-number	K073700
Device name	6F PROXIS SYSTEM
Applicant	St. Jude Medical, Inc.
Product code	DQY
Device class	Class II
Decision date	Oct 2, 2008
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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6F PROXIS SYSTEM

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