K-number	K001163
Device name	DMLC IV-ERGO
Applicant	3D Line USA, Inc.
Product code	IXI
Device class	Class II
Decision date	Oct 23, 2000
Decision	Substantially Equivalent
Regulation	892.5710

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View the full FDA submission: accessdata.fda.gov

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DMLC IV-ERGO

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