K-number	K150936
Device name	SureClip
Applicant	Conmed Corporation
Product code	FZP
Device class	Class II
Decision date	Oct 23, 2015
Decision	Substantially Equivalent
Regulation	878.4300

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Source

View the full FDA submission: accessdata.fda.gov

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SureClip

Everything you need for a 510(k) submission. Nothing you don't.