K-number	K781810
Device name	ELECTROSURGICAL UNIT 3001-3009
Applicant	Neomed Corp.
Product code	GEI
Device class	Class II
Decision date	Dec 20, 1978
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ELECTROSURGICAL UNIT 3001-3009

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