K-number	K082348
Device name	FIBERNET EMBOLIC PROTECTION SYSTEM
Applicant	Lumen Biomedical, Inc.
Product code	NTE
Device class	Class II
Decision date	Nov 18, 2008
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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FIBERNET EMBOLIC PROTECTION SYSTEM

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