K-number	K062525
Device name	REPROCESSED LIGASURE VESSEL SEALER/DIVIDER
Applicant	Ascent Healthcare Solutions
Product code	GEI
Device class	Class II
Decision date	May 16, 2007
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED LIGASURE VESSEL SEALER/DIVIDER

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