K-number	K082568
Device name	SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE
Applicant	Bovie Medical
Product code	GEI
Device class	Class II
Decision date	Nov 17, 2008
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE

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