K-number	K101711
Device name	CERULEAU ELECTROSURGICAL PROBE
Applicant	Nuortho Surgical, Inc.
Product code	GEI
Device class	Class II
Decision date	Jul 1, 2010
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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CERULEAU ELECTROSURGICAL PROBE

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