K-number	K072278
Device name	BRK TRANSSEPTAL NEEDLE
Applicant	St Jude Medical
Product code	DRC
Device class	Class II
Decision date	Sep 13, 2007
Decision	Substantially Equivalent
Regulation	870.1390

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Source

View the full FDA submission: accessdata.fda.gov

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BRK TRANSSEPTAL NEEDLE

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