K-number	K102439
Device name	FUNNEL GUIDE CATHETER MODEL G1020608
Applicant	Lazarus Effect, Inc.
Product code	DQY
Device class	Class II
Decision date	Jan 12, 2012
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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FUNNEL GUIDE CATHETER MODEL G1020608

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