K-number	K123532
Device name	OCELOT PIXL CATHETER
Applicant	Avinger, Inc.
Product code	PDU
Device class	Class II
Decision date	Dec 14, 2012
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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OCELOT PIXL CATHETER

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