K-number	K040763
Device name	RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE
Applicant	Resect Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	Apr 8, 2004
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE

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