K-number	K090661
Device name	NES REPROCESSED VARICOSE VEIN RF CATHETER
Applicant	Northeast Scientific, Inc.
Product code	NUJ
Device class	Class II
Decision date	Jul 21, 2010
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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NES REPROCESSED VARICOSE VEIN RF CATHETER

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