K-number	K111644
Device name	MOBICATH TRANSSEPTAL NEEDLE
Applicant	Great Batch Medical
Product code	DRC
Device class	Class II
Decision date	Oct 3, 2011
Decision	Substantially Equivalent
Regulation	870.1390

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Source

View the full FDA submission: accessdata.fda.gov

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MOBICATH TRANSSEPTAL NEEDLE

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