K-number	K081580
Device name	BEAMER ARGON SNARE PROBE
Applicant	Conmed Corporation
Product code	GEI
Device class	Class II
Decision date	Jun 19, 2008
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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BEAMER ARGON SNARE PROBE

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