K-number	K991601
Device name	DUAL LUMEN CATHETER, MODEL DL-35-90
Applicant	Endologix, Inc.
Product code	DQY
Device class	Class II
Decision date	Oct 28, 1999
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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DUAL LUMEN CATHETER, MODEL DL-35-90

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