K-number	K081138
Device name	SAFEFLO VENA CAVA FILTER
Applicant	Rmt Medical Technilogies, Inc.
Product code	DTK
Device class	Class II
Decision date	May 7, 2009
Decision	Unknown
Regulation	870.3375

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Source

View the full FDA submission: accessdata.fda.gov

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SAFEFLO VENA CAVA FILTER

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