K-number	K073326
Device name	NRG TRANSSEPTAL NEEDLE
Applicant	Baylis Medical Co., Inc.
Product code	DXF
Device class	Class II
Decision date	May 28, 2008
Decision	Substantially Equivalent
Regulation	870.5175

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Source

View the full FDA submission: accessdata.fda.gov

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NRG TRANSSEPTAL NEEDLE

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