K-number	K122949
Device name	MEDLINE SUCTION COAGULATOR
Applicant	Medline Industries, Inc.
Product code	GEI
Device class	Class II
Decision date	Oct 16, 2013
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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MEDLINE SUCTION COAGULATOR

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