K-number	K011562
Device name	LUMEND PERCUTANEOUS CATHETER
Applicant	Lumend, Inc.
Product code	DQY
Device class	Class II
Decision date	Jan 16, 2002
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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LUMEND PERCUTANEOUS CATHETER

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