K-number	K901235
Device name	GREENFIELD VENA CAVA FILTER W/19.5 FR INTRODUCER
Applicant	Boston Scientific Corp
Product code	DTK
Device class	Class II
Decision date	Oct 9, 1990
Decision	Substantially Equivalent
Regulation	870.3375

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View the full FDA submission: accessdata.fda.gov

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GREENFIELD VENA CAVA FILTER W/19.5 FR INTRODUCER

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